FDA 510(k)

Disposable Radiofrequency Cannula

Número K: K253907 · 2026-04-16

Data da decisão2026-04-16

Código do produtoGXI

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Radiofrequency Cannula is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-04-16 under 510(k) number K253907. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Radiofrequency Cannula?

Disposable Radiofrequency Cannula is a medical device that received FDA 510(k) clearance on 2026-04-16. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K253907.

When did Disposable Radiofrequency Cannula receive FDA 510(k) clearance?

Disposable Radiofrequency Cannula received FDA 510(k) clearance on 2026-04-16, under 510(k) number K253907.

Who is the listed applicant for Disposable Radiofrequency Cannula?

The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Radiofrequency Cannula?

The FDA product code for Disposable Radiofrequency Cannula is GXI.

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Fonte oficial

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