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FDA 510(k)

GYNESCOPE LAPAROSCOPIC FORCEPS

K-Number: K902657 · 1990-09-19

ApplicantGynescope Corp.
Decision Date1990-09-19
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GYNESCOPE LAPAROSCOPIC FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Gynescope Corp.. It received FDA 510(k) clearance on 1990-09-19 under 510(k) number K902657. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYNESCOPE LAPAROSCOPIC FORCEPS?

GYNESCOPE LAPAROSCOPIC FORCEPS is a medical device that received FDA 510(k) clearance on 1990-09-19. The listed applicant is Gynescope Corp.. The 510(k) number is K902657.

When did GYNESCOPE LAPAROSCOPIC FORCEPS receive FDA 510(k) clearance?

GYNESCOPE LAPAROSCOPIC FORCEPS received FDA 510(k) clearance on 1990-09-19, under 510(k) number K902657.

Who is the listed applicant for GYNESCOPE LAPAROSCOPIC FORCEPS?

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

What is the FDA product code for GYNESCOPE LAPAROSCOPIC FORCEPS?

The FDA product code for GYNESCOPE LAPAROSCOPIC FORCEPS is HET.

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Other records listing Gynescope 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.

K902658GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODESK901530WALLACE INTRAUTERINE INSEMINATION CATHETERK902655GYNESCOPE LAPAROSCOPESK902656GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVESK902049CROAK OVARIAN BIOPSY FORCEPK902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS

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Related Devices (Code: HET)

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.

K250939SIRIUS Endoscope System (PR-SI-1230)Precision Robotics (Hong Kong) LimitedK243821i-CutA.M.I. Agency For Medical Innovations GmbHK221642SIRIUS Endoscope SystemPrecision Robotics (Hong Kong) LimitedK210116Video Endoscopy System, 3D Video Endoscopy SystemSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.K201832Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5Olympus Medical Systems Corp.K210104SurroundScope System270surgical , 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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