FDA 510(k)

Disposable Semi Automatic Biopsy Instrument

Número K: K212820 · 2022-07-06

RequerenteSuzhou Leapmed Healthcare Corporation

Data da decisão2022-07-06

Código do produtoKNW

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Semi Automatic Biopsy Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Leapmed Healthcare Corporation. It received FDA 510(k) clearance on 2022-07-06 under 510(k) number K212820. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Semi Automatic Biopsy Instrument?

Disposable Semi Automatic Biopsy Instrument is a medical device that received FDA 510(k) clearance on 2022-07-06. The listed applicant is Suzhou Leapmed Healthcare Corporation. The 510(k) number is K212820.

When did Disposable Semi Automatic Biopsy Instrument receive FDA 510(k) clearance?

Disposable Semi Automatic Biopsy Instrument received FDA 510(k) clearance on 2022-07-06, under 510(k) number K212820.

Who is the listed applicant for Disposable Semi Automatic Biopsy Instrument?

The FDA 510(k) record lists Suzhou Leapmed Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Semi Automatic Biopsy Instrument?

The FDA product code for Disposable Semi Automatic Biopsy Instrument is KNW.

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Outros registros que listam Suzhou Leapmed Healthcare Corporation como candidato(a)

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Fonte oficial

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