FIJI SUN FLUORESCENT TANNING UNIT— 510(k) K151721

Name: FDA 510(k) clearance K151721
Creator: U.S. Food and Drug Administration
Published: 2018-06-22

Substantially Equivalent

Kdb Inc. (Dba) Sperti Sunlamp

FDA 510(k) clearance K151721 for FIJI SUN FLUORESCENT TANNING UNIT, Substantially Equivalent on 2018-06-22. Applicant: Kdb Inc. (Dba) Sperti Sunlamp. Device class: 2.

Clearance details

Applicant: Kdb Inc. (Dba) Sperti Sunlamp
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 2015-06-25
Decision date: 2018-06-22
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Crescent Springs, KY, 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.