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ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY

K935235 Class II Traditional
Decision Date
1995-03-23
Sponsor / Applicant
Smith & Nephew Richards, Inc.

Technical Specification

510(k) Submission ID K935235
Product Code GCM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1995-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY received FDA 510(k) clearance under submission number K935235, sponsored by Smith & Nephew Richards, 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 1995-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code GCM and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.