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FDA 510(k)

BIOPSY FORCEPS

K-Number: K871710 · 1987-08-10

ApplicantFrantz Medical Development, Ltd.
Decision Date1987-08-10
Product CodeFCL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Frantz Medical Development, Ltd.. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K871710. The device is classified under product code FCL. It was reviewed by the GU 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 1987-08-10. The listed applicant is Frantz Medical Development, Ltd.. The 510(k) number is K871710.

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

BIOPSY FORCEPS received FDA 510(k) clearance on 1987-08-10, under 510(k) number K871710.

Who is the listed applicant for BIOPSY FORCEPS?

The FDA 510(k) record lists Frantz Medical Development, Ltd. 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 FCL.

Related Clinical Trials

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.

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Other records listing Frantz Medical Development, Ltd. 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.

K981541CLEARSTAR ENTERAL NUTRITION PUMPK905282ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCEK873119FLEXIFLO COMPANION ENTERAL NUTRITION PUMPK863508FRANTZ MEDICAL ELECTRODE

Related Devices (Code: FCL)

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.

K032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEOlympus Optical Co., Ltd.K973611SPECTRASCIENCE REUSABLE BIOPSY FORCEPSSpectrascience, Inc.K971315AUXILIARY INSTRUMENTS FOR URSRichard Wolf Medical Instruments Corp.K964120INJECTO FLUSHRobert J. Jynch, Jr.K963517SPECTRA SCIENCE BIOPSY FORCEPSSpectrascience, Inc.K955065OLYMPUS FB SERIES BIOPSY FORCEPSOlympus America, Inc.

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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