ENDOSCOPIC CAMERA TV W/AUDIO— 510(k) K832342

Name: FDA 510(k) clearance K832342
Creator: U.S. Food and Drug Administration
Published: 1983-09-12

Substantially Equivalent

Kamiya Tsusan Kaisha, Ltd.

FDA 510(k) clearance K832342 for ENDOSCOPIC CAMERA TV W/AUDIO, Substantially Equivalent on 1983-09-12. Applicant: Kamiya Tsusan Kaisha, Ltd.. Device class: 1.

Clearance details

Applicant: Kamiya Tsusan Kaisha, Ltd.
Product code: Code KQM
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1983-07-12
Decision date: 1983-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo 100-91 Japan, US

Download summary PDF View on FDA.gov ↗

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