BR-S601MU (SURGICAL VIDEO RECORDER)— 510(k) K890119

Name: FDA 510(k) clearance K890119
Creator: U.S. Food and Drug Administration
Published: 1989-01-24

Substantially Equivalent

Victor Co. of Japan, Ltd. C/O Jvc Corp.

FDA 510(k) clearance K890119 for BR-S601MU (SURGICAL VIDEO RECORDER), Substantially Equivalent on 1989-01-24. Applicant: Victor Co. of Japan, Ltd. C/O Jvc Corp.. Device class: 1.

Clearance details

Applicant: Victor Co. of Japan, Ltd. C/O Jvc Corp.
Product code: Code FWC
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1989-01-11
Decision date: 1989-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elmwood Park, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.