meddevicedb.com FDA Device Reference

AUTO SUTURE* STERILIZATION TRAY**

K954090 Class II Traditional
Decision Date
1995-11-22
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K954090
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1995-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE* STERILIZATION TRAY** received FDA 510(k) clearance under submission number K954090, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1995-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.