meddevicedb.com FDA Device Reference

AUTO SUTURE(R) ENDOSCOPIC CLAMP

K903205 Class II Traditional
Decision Date
1990-10-11
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K903205
Product Code HDA
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4400
Decision Date 1990-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO SUTURE(R) ENDOSCOPIC CLAMP received FDA 510(k) clearance under submission number K903205, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1990-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code HDA and 21 CFR 884.4400, within the Obstetrics/Gynecology review panel as a Class II device.