meddevicedb.com FDA Device Reference

SURGICAL RETRACTOR KIT

K940193 Class II Traditional
Decision Date
1994-02-15
Sponsor / Applicant
Advanced Surgical, Inc.

Technical Specification

510(k) Submission ID K940193
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1994-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL RETRACTOR KIT received FDA 510(k) clearance under submission number K940193, sponsored by Advanced Surgical, Inc.. 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 1994-02-15.

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.