meddevicedb.com FDA Device Reference

3 FRENCH FLEXIBLE BIOPSY FORCEPS

K881399 Class II Traditional
Decision Date
1988-04-11
Sponsor / Applicant
Cook Urological, Inc.

Technical Specification

510(k) Submission ID K881399
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1988-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3 FRENCH FLEXIBLE BIOPSY FORCEPS received FDA 510(k) clearance under submission number K881399, sponsored by Cook Urological, Inc.. 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 1988-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code OCZ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.