meddevicedb.com FDA Device Reference

BIPOLAR BIOPSY FORCEPS

K904985 Class II Traditional
Decision Date
1991-01-25
Sponsor / Applicant
Everest Medical Corp.

Technical Specification

510(k) Submission ID K904985
Product Code KGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 1991-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIPOLAR BIOPSY FORCEPS received FDA 510(k) clearance under submission number K904985, sponsored by Everest Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1991-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code KGE and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.