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ENDOSCOPIC CAMERA TV W/AUDIO

K832342 Class I Traditional
Decision Date
1983-09-12
Sponsor / Applicant
Kamiya Tsusan Kaisha, Ltd.

Technical Specification

510(k) Submission ID K832342
Product Code KQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1983-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPIC CAMERA TV W/AUDIO received FDA 510(k) clearance under submission number K832342, sponsored by Kamiya Tsusan Kaisha, Ltd.. 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 1983-09-12.

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.