CABANNA TAN SUNLAMP— 510(k) K801925

Name: FDA 510(k) clearance K801925
Creator: U.S. Food and Drug Administration
Published: 1980-10-03

Substantially Equivalent

The Marketing Exchange, Inc.

FDA 510(k) clearance K801925 for CABANNA TAN SUNLAMP, Substantially Equivalent on 1980-10-03. Applicant: The Marketing Exchange, Inc.. Device class: 2.

Clearance details

Applicant: The Marketing Exchange, Inc.
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 1980-08-12
Decision date: 1980-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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