meddevicedb.com FDA Device Reference

AUTO SUTURE SUTURE CLOSURE

K954853 Class II Traditional
Decision Date
1995-12-20
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K954853
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1995-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE SUTURE CLOSURE received FDA 510(k) clearance under submission number K954853, 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 1995-12-20.

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.