SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1— 510(k) K800744

Name: FDA 510(k) clearance K800744
Creator: U.S. Food and Drug Administration
Published: 1980-06-04

Substantially Equivalent

Sun Ind., Inc.

FDA 510(k) clearance K800744 for SUNTANA SUNBED #SB-1 & SUNBRELLA #SU-1, Substantially Equivalent on 1980-06-04. Applicant: Sun Ind., Inc.. Device class: 2.

Clearance details

Applicant: Sun Ind., Inc.
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 1980-04-03
Decision date: 1980-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.