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FDA 510(k)

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

K-Number: K252050 · 2026-03-20

ApplicantOlympus Medical Systems Corporation
Decision Date2026-03-20
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Olympus Medical Systems Corporation. The 510(k) number is K252050.

When was Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D approved by the FDA?

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

What company makes Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D?

Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D is manufactured by Olympus Medical Systems Corporation.

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.

Related Clinical Trials

NCT06824402 Cryoprobe Biopsy and Chronic Rejection in Lung Transplant Recipients RECRUITING NCT05751278 Cryoprobe Versus Forceps for Transbronchial Biopsy COMPLETED

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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