PHILIPS UVA (/09) AND PHILIPS UVA-1 (/10) ULTRAVIOLET LAMPS— 510(k) K130519

Name: FDA 510(k) clearance K130519
Creator: U.S. Food and Drug Administration
Published: 2013-12-24

Substantially Equivalent

Philips Lighting Company

FDA 510(k) clearance K130519 for PHILIPS UVA (/09) AND PHILIPS UVA-1 (/10) ULTRAVIOLET LAMPS, Substantially Equivalent on 2013-12-24. Applicant: Philips Lighting Company. Device class: 2.

Clearance details

Applicant: Philips Lighting Company
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 2013-02-27
Decision date: 2013-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salina, KS, US

Download summary PDF View on FDA.gov ↗

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