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FDA 510(k)

BIOPSY FORCEPS

K-Number: K834095 · 1984-01-27

ApplicantMicro Vasive, Inc.
Decision Date1984-01-27
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Micro Vasive, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K834095. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY FORCEPS?

BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Micro Vasive, Inc.. The 510(k) number is K834095.

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

BIOPSY FORCEPS received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834095.

Who is the listed applicant for BIOPSY FORCEPS?

The FDA 510(k) record lists Micro Vasive, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPSY FORCEPS?

The FDA product code for BIOPSY FORCEPS is GEN.

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Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900948GS-1002 GRASPING FORCEP, 5MM WITH RATCHETSolos Endoscopy, Inc.

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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