FREE SUN PRO DESIGN 3000 AND 3800— 510(k) K925171

Name: FDA 510(k) clearance K925171
Creator: U.S. Food and Drug Administration
Published: 1992-12-29

Substantially Equivalent

Free Sun Prod. AB

FDA 510(k) clearance K925171 for FREE SUN PRO DESIGN 3000 AND 3800, Substantially Equivalent on 1992-12-29. Applicant: Free Sun Prod. AB. Device class: 2.

Clearance details

Applicant: Free Sun Prod. AB
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1992-10-14
Decision date: 1992-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Uppsala, Sweden, SE

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