meddevicedb.com FDA Device Reference

BICOAG COAGULATING FORCEPS

K971565 Class II Traditional
Decision Date
1998-03-12
Sponsor / Applicant
Everest Medical Corp.

Technical Specification

510(k) Submission ID K971565
Product Code HIN
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4150
Decision Date 1998-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BICOAG COAGULATING FORCEPS received FDA 510(k) clearance under submission number K971565, sponsored by Everest Medical 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 1998-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code HIN and 21 CFR 884.4150, within the Obstetrics/Gynecology review panel as a Class II device.