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FDA 510(k)

MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS

K-Number: K902019 · 1990-06-07

ApplicantGynescope Corp.
Decision Date1990-06-07
Product CodeHDF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFIED METAL SPECULUM & SPECIAL BULLET 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 1990-06-07 under 510(k) number K902019. The device is classified under product code HDF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS?

MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS is a medical device that received FDA 510(k) clearance on 1990-06-07. The listed applicant is Gynescope Corp.. The 510(k) number is K902019.

When did MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS receive FDA 510(k) clearance?

MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS received FDA 510(k) clearance on 1990-06-07, under 510(k) number K902019.

Who is the listed applicant for MODIFIED METAL SPECULUM & SPECIAL BULLET 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 MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS?

The FDA product code for MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS is HDF.

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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 ELECTRODESK902657GYNESCOPE LAPAROSCOPIC FORCEPSK901530WALLACE INTRAUTERINE INSEMINATION CATHETERK902655GYNESCOPE LAPAROSCOPESK902656GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVESK902049CROAK OVARIAN BIOPSY FORCEP

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Related Devices (Code: HDF)

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.

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTThomasville Medical Assoc.K891041MIYA SPECULUMZinnanti Surgical Instruments, Inc.K891044LASER SPECULAZinnanti Surgical Instruments, Inc.K890375VAGINAL SPECULUMKinetic Medical ProductsK862478HAYES VAGINAL SHIELDFranklin Medical USA, Inc.K853640WELLINGTON HOSPITAL PATTERN SELF RETAINING VAGINALDowns Surgical , 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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