ULTRABRONZ SERIES 400 TANNING BED— 510(k) K931660

Name: FDA 510(k) clearance K931660
Creator: U.S. Food and Drug Administration
Published: 1993-12-17

Substantially Equivalent

Eurocut, Ltd.

FDA 510(k) clearance K931660 for ULTRABRONZ SERIES 400 TANNING BED, Substantially Equivalent on 1993-12-17. Applicant: Eurocut, Ltd.. Device class: 2.

Clearance details

Applicant: Eurocut, Ltd.
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 1993-04-05
Decision date: 1993-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Agoura, CA, 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.