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FDA 510(k)

CROAK OVARIAN BIOPSY FORCEP

K-Number: K902049 · 1990-06-07

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

Device Summary

CROAK OVARIAN BIOPSY FORCEP 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 K902049. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROAK OVARIAN BIOPSY FORCEP?

CROAK OVARIAN BIOPSY FORCEP 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 K902049.

When did CROAK OVARIAN BIOPSY FORCEP receive FDA 510(k) clearance?

CROAK OVARIAN BIOPSY FORCEP received FDA 510(k) clearance on 1990-06-07, under 510(k) number K902049.

Who is the listed applicant for CROAK OVARIAN BIOPSY FORCEP?

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 CROAK OVARIAN BIOPSY FORCEP?

The FDA product code for CROAK OVARIAN BIOPSY FORCEP is HFB.

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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 SLEEVESK902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS

View all 9 devices →

Related Devices (Code: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische InstrumenteK930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.

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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