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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 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.

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. 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.

Other records listing Olympus Medical Systems Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S (TB-0520FCS)K261260HD Camera Head OLYMPUS CH-S200-08-LBK260580Single Use Reloadable Clip Applicator (HX-810LR, HX-810UR); Clip (HX-610-090, HX-610-135); Long Clip (HX-610-090L, HX-610-135L); Short Clip (HX-610-090S, HX-610-135S); Super Short Clip (HX-610-135XS)K252341EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-Q190); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-H190 ); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH190)K251807Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR

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Related Devices (Code: EOB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261544Hydro Irrigation SystemStryker InstrumentsK254133ENTity USB Videoscope SystemOptim, LLCK253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)Zhuhai Wesee Meditech Co., Ltd.K241731Outlook Surgical Versa One System (8900139)Resnent, LLCK243639Portare System (FA-001)Grumpy Innovation, Inc.K243380VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500 (OLYMPUS OTV-S500)Olympus Medical Systems Corporation

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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