meddevicedb.com FDA Device Reference

MANUAL SURGICAL INSTRUMENTS

K921925 Class II Traditional
Decision Date
1993-05-26
Sponsor / Applicant
3M Health Care, Ltd.

Technical Specification

510(k) Submission ID K921925
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1993-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MANUAL SURGICAL INSTRUMENTS received FDA 510(k) clearance under submission number K921925, sponsored by 3M Health Care, Ltd.. 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 1993-05-26.

Classification & Regulation

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