EUROTAN BY AYK— 510(k) K860489

Name: FDA 510(k) clearance K860489
Creator: U.S. Food and Drug Administration
Published: 1986-02-24

Substantially Equivalent for Some Indications

Eurotan Intl.

FDA 510(k) clearance K860489 for EUROTAN BY AYK, Substantially Equivalent for Some Indications on 1986-02-24. Applicant: Eurotan Intl.. Device class: 2.

Clearance details

Applicant: Eurotan Intl.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-02-10
Decision date: 1986-02-24
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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