meddevicedb.com FDA Device Reference

AUTO SUTURE MODIFIED GRIP

K942885 Class II Traditional
Decision Date
1994-08-22
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K942885
Product Code FBQ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5090
Decision Date 1994-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE MODIFIED GRIP received FDA 510(k) clearance under submission number K942885, sponsored by United States Surgical, A Division of Tyco Healthc. 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 1994-08-22.

Classification & Regulation

This clearance is catalogued under FDA product code FBQ and 21 CFR 876.5090, within the Gastroenterology, Urology review panel as a Class II device.