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FDA 510(k)

BIPOLAR BIOPSY FORCEPS

K-Number: K904985 · 1991-01-25

ApplicantEverest Medical Corp.
Decision Date1991-01-25
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BIPOLAR BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Everest Medical Corp.. It received FDA 510(k) clearance on 1991-01-25 under 510(k) number K904985. 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 BIPOLAR BIOPSY FORCEPS?

BIPOLAR BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Everest Medical Corp.. The 510(k) number is K904985.

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

BIPOLAR BIOPSY FORCEPS received FDA 510(k) clearance on 1991-01-25, under 510(k) number K904985.

Who is the listed applicant for BIPOLAR BIOPSY FORCEPS?

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

What is the FDA product code for BIPOLAR BIOPSY FORCEPS?

The FDA product code for BIPOLAR BIOPSY FORCEPS is KGE.

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Other records listing Everest Medical Corp. 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.

K003060PLASMAKINETIC GENERATORK000496EVERSHEARS BIPOLAR SCISSORSK993412BITX PROBESK994336BITX PROBESK971565BICOAG COAGULATING FORCEPSK955001EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS

View all 21 devices →

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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