SUNFIT, ULTRA VIOLET LAMPS AND SUNLAMP PRODUCTS— 510(k) K861533

Name: FDA 510(k) clearance K861533
Creator: U.S. Food and Drug Administration
Published: 1986-05-08

Substantially Equivalent

Sunfit, Inc.

FDA 510(k) clearance K861533 for SUNFIT, ULTRA VIOLET LAMPS AND SUNLAMP PRODUCTS, Substantially Equivalent on 1986-05-08. Applicant: Sunfit, Inc.. Device class: 2.

Clearance details

Applicant: Sunfit, Inc.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-04-24
Decision date: 1986-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Rochelle, NY, US

Download summary PDF View on FDA.gov ↗

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