# Why do RF frequency records differ across sources?

> A conflicting specification remains a set of source-specific observations until model, source identity and document sections are matched.

Oligio X has different frequency statements across a regulator-filed summary, a global manufacturer page and an unverified-affiliation commercial page. A single frequency or power ranking would hide those differences.

Written by the Monun Device Research Group editorial team on October 25, 2026. Canonical address: https://kliftingdevices.site/articles/frequency-conflicts.

## What is an RF specification observation?

It is a value retained with its unit, source, model scope and reading location.

A number without its origin can look definitive even when it came from a regional advertisement. Recording the source role separates a regulator-filed technical statement from a commercial description. It also preserves what was actually read instead of treating a downloaded file as a complete document review.

**Oligio X source-specific observations; research 2026-10-24**

| Source | Value | Unit | Location read | Unresolved limit |
| --- | --- | --- | --- | --- |
| K243929 | 6.78 | MHz | §5 Description; §7 comparison; Performance Testing | FDA-filed applicant summary; not a Korean specification |
| WON-X | 6.78 | MHz | Global manufacturer product specifications | Manufacturer statement; exact market configuration not matched |
| BRANDED-US-CONFLICT | 448 | kHz | US-branded commercial page specifications | Corporate affiliation unverified; not authenticated as a WONTECH office |
| K243929 | 200 | W | §5 Description of the Device | Differs from the comparison and performance sections; no single rating selected |
| K243929 | 140 | W | §7 Max output power; Non-Clinical Test Summary / 4) Performance Testing | Differs from §5; source clarification not obtained |

## Why verify a branded commercial page’s affiliation?

A familiar logo or domain wording does not independently verify the page’s corporate relationship.

The US-branded Oligio X page was retained as an observed commercial statement with affiliation unverified. It is not described as a conflict between two authenticated manufacturer offices. This limit matters because corporate authentication and the accuracy of a technical statement are different questions.

## Is every part of an FDA PDF written by FDA?

The decision letter and applicant-submitted technical summary have different authorship roles within the same file.

The decision letter establishes the regulatory event. A technical summary describes the submitted device. Keeping those roles separate prevents a technical comparison from becoming a regulator’s independent clinical performance claim. The document location remains useful even when both sections are relevant.

## Can a single PDF contain differing specifications?

The selected Oligio X file contains differing maximum-power descriptions across its technical sections.

The difference is retained as an unresolved observation. A larger number is not chosen merely because it sounds more capable. A device description, comparison table and performance statement can refer to different contexts; the exact interpretation requires a source-level clarification that this catalog has not obtained.

**Responses to a specification disagreement**

| Observation | Permitted response | Avoided conclusion |
| --- | --- | --- |
| Different sources | Retain each source and affiliation state | Both are authenticated offices |
| Different sections | Keep locations and wording | Choose the larger value |
| Different units | Show the original unit | Average unlike specifications |
| No clarification | Mark unresolved | Call the device strongest or unsafe |

## Does equal RF frequency mean equal treatment?

Frequency alone does not match circuit, electrode, operating conditions or clinical protocol.

Even a correctly identified frequency is only one technical field. Surface contact, needle delivery, tip geometry and mode can differ. The catalog therefore does not convert one device’s shot count, power or frequency into an equivalent dose on another device.

## Which identity fields come before unit conversion?

The source must first refer to the same model, market configuration and operating context.

A unit conversion can express the same quantity in another unit, but it cannot authenticate the source or prove that two statements describe the same configuration. The model suffix, applicator and technical section remain attached. The uncertainty is preserved instead of being hidden by a mathematically tidy display.

## What does the RF conflict record help a reader ask?

It identifies the model, source and section requiring clarification without giving a treatment verdict.

A reader can ask which current local label or instruction supports the quoted specification. The unresolved conflict can then be followed to a document revision or corrected source statement. Until that evidence arrives, the record remains unresolved and the dated observations remain available.

## What else do people ask about RF frequency conflicts?

### Does the catalog choose one Oligio X frequency?

The conflicting observations remain source-specific; no single unqualified value is selected.

### Is the US-branded page an authenticated office?

Its corporate affiliation was not verified in the research.

### Can unit conversion resolve identity?

It changes units, not model identity, affiliation or document scope.

### Is a larger wattage automatically better?

The records do not support a treatment-performance ranking from raw wattage.

### Does conflict prove a device is unsafe?

It marks an unresolved source relationship, without making a device safety verdict.

## What should you read next?

- [What does FDA clearance mean for a lifting device?](https://kliftingdevices.site/articles/clearance-and-approval)
- [Which models and lots does a device recall cover?](https://kliftingdevices.site/articles/recall-scope)
- [Korea lifting model lookup](https://kliftingdevices.site/tools/model-finder)
- [Korea device indication checks](https://kliftingdevices.site/tools/claim-checker)

## Where do these numbers come from?

- [K243929 : Oligio X](https://www.accessdata.fda.gov/cdrh_docs/pdf24/K243929.pdf) - U.S. Food and Drug Administration
- [wontech - products view](https://wontech.com/eng/product/view.php?product_id=27) - WONTECH
- [OLIGIO-X : Next-Generation Monopolar RF Platform | WONTECH USA](https://wontechusa.com/products/oligio-x) - Commercial website; corporate affiliation unverified