meddevicedb.com FDA Device Reference

RETRIEVABLE FORCEPS

K792345 Class II Traditional
Decision Date
1979-12-20
Sponsor / Applicant
Mill-Rose Laboratory

Technical Specification

510(k) Submission ID K792345
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1979-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RETRIEVABLE FORCEPS received FDA 510(k) clearance under submission number K792345, sponsored by Mill-Rose Laboratory. 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 1979-12-20.

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.