HYDRASOLVE LIPOPLASTY SYSTEM— 510(k) K130152

Name: FDA 510(k) clearance K130152
Creator: U.S. Food and Drug Administration
Published: 2013-04-18

Substantially Equivalent

Andrew Technologies, LLC

FDA 510(k) clearance K130152 for HYDRASOLVE LIPOPLASTY SYSTEM, Substantially Equivalent on 2013-04-18. Applicant: Andrew Technologies, LLC. Device class: 2.

Clearance details

Applicant: Andrew Technologies, LLC
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2013-01-22
Decision date: 2013-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haddonfield, NJ, US

Download summary PDF View on FDA.gov ↗

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