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FDA 510(k)

REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS

K-Number: K022751 · 2002-11-04

ApplicantMedical Device Services
Decision Date2002-11-04
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Services. It received FDA 510(k) clearance on 2002-11-04 under 510(k) number K022751. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS?

REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 2002-11-04. The listed applicant is Medical Device Services. The 510(k) number is K022751.

When did REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS receive FDA 510(k) clearance?

REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS received FDA 510(k) clearance on 2002-11-04, under 510(k) number K022751.

Who is the listed applicant for REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS?

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

What is the FDA product code for REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS?

The FDA product code for REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS is KGE.

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Other records listing Medical Device Services 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.

K022753REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPSK022748REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERSK022743REPROCESSED DISPOSABLE TROCARSK022744REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS

Related Devices (Code: KGE)

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.

K251807Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LROlympus Medical Systems Corp.K250187Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)Olympus Medical Systems CorporationK242857ClearHemograsperFinemedix Co., Ltd.K231721Disposable Hot Biopsy ForcepsBeijing Zksk Technology Co., Ltd.K220053Diathermic Slitter (FlushKnife) DK2620JI and DK2623JIFujifilm CorporationK210406Bipolar Coagulation ForecepsHangzhou AGS MedTech Co., Ltd.

Official Source

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

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