FDA 510(k)

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D

Número K: K252050 · 2026-03-20

RequerenteOlympus Medical Systems Corporation

Data da decisão2026-03-20

Código do produtoEOB

Comité consultivoEN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K252050. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K252050.

When did Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D receive FDA 510(k) clearance?

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D received FDA 510(k) clearance on 2026-03-20, under 510(k) number K252050.

Who is the listed applicant for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

The FDA 510(k) record lists Olympus Medical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

The FDA product code for Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is EOB.

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Fonte oficial

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