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FDA 510(k)

RESUABLE HOT BIOPSY FORCEPS

K-Number: K972505 · 1997-09-18

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1997-09-18
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RESUABLE HOT BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1997-09-18 under 510(k) number K972505. 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 RESUABLE HOT BIOPSY FORCEPS?

RESUABLE HOT BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1997-09-18. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K972505.

When did RESUABLE HOT BIOPSY FORCEPS receive FDA 510(k) clearance?

RESUABLE HOT BIOPSY FORCEPS received FDA 510(k) clearance on 1997-09-18, under 510(k) number K972505.

Who is the listed applicant for RESUABLE HOT BIOPSY FORCEPS?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESUABLE HOT BIOPSY FORCEPS?

The FDA product code for RESUABLE HOT BIOPSY FORCEPS is KGE.

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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

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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