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FDA 510(k)

GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES

K-Number: K902658 · 1990-09-19

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

Device Summary

GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES 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 K902658. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES?

GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES 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 K902658.

When did GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES receive FDA 510(k) clearance?

GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES received FDA 510(k) clearance on 1990-09-19, under 510(k) number K902658.

Who is the listed applicant for GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES?

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 MONOPOLAR FORCEPS AND ELECTRODES?

The FDA product code for GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES is KNF.

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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.

K902657GYNESCOPE LAPAROSCOPIC FORCEPSK901530WALLACE INTRAUTERINE INSEMINATION CATHETERK902655GYNESCOPE LAPAROSCOPESK902656GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVESK902049CROAK OVARIAN BIOPSY FORCEPK902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS

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Related Devices (Code: KNF)

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.

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KGK250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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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