Clearance Summary
GAYLOR-THOMS UTERINE BIOPSY FORCEPS 1810-144 PCS. received FDA 510(k) clearance under submission number K851110, sponsored by The Huxley Instrument Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1985-04-08.
- Submission: K851110
- Applicant / Sponsor: The Huxley Instrument Corp.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4530
- Decision date: 1985-04-08
Classification & Regulation
This clearance is catalogued under FDA product code HFB and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class I device.