meddevicedb.com FDA Device Reference

SURGICAL CAMERA ACCESSORIES

K871595 Class I Traditional
Decision Date
1987-05-07
Sponsor / Applicant
M.P. Video, Inc.

Technical Specification

510(k) Submission ID K871595
Product Code KQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1987-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL CAMERA ACCESSORIES received FDA 510(k) clearance under submission number K871595, sponsored by M.P. Video, 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 1987-05-07.

Classification & Regulation

This clearance is catalogued under FDA product code KQM and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.