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THE COUPLER/DRAPE(TM), VIDEO CAMERA STERILE DRAPE

K945656 Class II Traditional
Decision Date
1995-03-28
Sponsor / Applicant
Micro-Medical Devices, Inc.

Technical Specification

510(k) Submission ID K945656
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1995-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE COUPLER/DRAPE(TM), VIDEO CAMERA STERILE DRAPE received FDA 510(k) clearance under submission number K945656, sponsored by Micro-Medical Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1995-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.