PHOTOTHERAPEUTIX MODEL 3200A— 510(k) K935524

Name: FDA 510(k) clearance K935524
Creator: U.S. Food and Drug Administration
Published: 1995-02-17

Substantially Equivalent

Avex Industries , Ltd.

FDA 510(k) clearance K935524 for PHOTOTHERAPEUTIX MODEL 3200A, Substantially Equivalent on 1995-02-17. Applicant: Avex Industries , Ltd.. Device class: 2.

Clearance details

Applicant: Avex Industries , Ltd.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1993-11-16
Decision date: 1995-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hudson Falls, NY, US

Download summary PDF View on FDA.gov ↗

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