Medical Device Manufacturer · US , Willoughby , OH

Gynescope Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1990

Total

Cleared

Denied

Gynescope Corp. has 9 FDA 510(k) cleared medical devices. Based in Willoughby, US.

Historical record: 9 cleared submissions from 1990 to 1990. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Gynescope Corp. Filter by specialty or product code using the sidebar.

Gynescope Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gynescope Corp.

9 devices

1-9 of 9

Cleared Sep 19, 1990

GYNESCOPE LAPAROSCOPIC FORCEPS

K902657 · HET

Obstetrics & Gynecology · 96d

Cleared Sep 19, 1990

GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODES

K902658 · KNF

Obstetrics & Gynecology · 96d

Cleared Jul 23, 1990

WALLACE INTRAUTERINE INSEMINATION CATHETER

K901530 · EJT

Dental · 112d

Cleared Jul 13, 1990

GYNESCOPE LAPAROSCOPES

K902655 · HET

Obstetrics & Gynecology · 28d

Cleared Jun 29, 1990

GYNESCOPE LAPAROSCOPIC TROCARS AND SLEEVES

K902656 · HET

Obstetrics & Gynecology · 14d

Cleared Jun 07, 1990

MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPS

K902019 · HDF

Obstetrics & Gynecology · 35d

Cleared Jun 07, 1990

CROAK OVARIAN BIOPSY FORCEP

K902049 · HFB

Obstetrics & Gynecology · 31d

Cleared May 07, 1990

OTT INSUFFLATION FILTER TUBING

K900878 · HIF

Obstetrics & Gynecology · 70d

Cleared Mar 05, 1990

GYNECOLOGICAL INSTRUMENTATION

K895225 · HET

Obstetrics & Gynecology · 203d

Gynescope Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gynescope Corp.

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