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FDA 510(k)

OVAL CUP BIOPSY FORCEP

K-Number: K911155 · 1991-08-07

ApplicantEndovations
Decision Date1991-08-07
Product CodeFCF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OVAL CUP BIOPSY FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Endovations. It received FDA 510(k) clearance on 1991-08-07 under 510(k) number K911155. The device is classified under product code FCF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVAL CUP BIOPSY FORCEP?

OVAL CUP BIOPSY FORCEP is a medical device that received FDA 510(k) clearance on 1991-08-07. The listed applicant is Endovations. The 510(k) number is K911155.

When did OVAL CUP BIOPSY FORCEP receive FDA 510(k) clearance?

OVAL CUP BIOPSY FORCEP received FDA 510(k) clearance on 1991-08-07, under 510(k) number K911155.

Who is the listed applicant for OVAL CUP BIOPSY FORCEP?

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

What is the FDA product code for OVAL CUP BIOPSY FORCEP?

The FDA product code for OVAL CUP BIOPSY FORCEP is FCF.

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Other records listing Endovations 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.

K955413ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETERK942110INJECT-SNAREK934315ENDOVATIONS(R) .035 PRE-CUT PAPILLATOMEK9138412 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATHK9138705MM MICROSCISSORSK892218ENDO-SPONGE

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Related Devices (Code: FCF)

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.

K070759POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEMVidacare CorporationK062833POWERED EZ-IO BONE MARROW ASPIRATION SYSTEMVidacare CorporationK984168BARRETT'S ESOPHAGEAL CYTOLOGY DEVICEUnited States Endoscopy Group, Inc.K915142AMCATH DISPOSABLE BIOPSY FORCEPSIntl. Medical, Inc.K843477PHARMA-PLAST RECTAL TIPZimmar Consulting , 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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