Alma LipoFlow System— 510(k) K171242

Substantially Equivalent

Alma Lasers, Inc.

FDA 510(k) clearance K171242 for Alma LipoFlow System, Substantially Equivalent on 2017-07-14. Applicant: Alma Lasers, Inc.. Device class: 2.

Clearance details

Applicant: Alma Lasers, Inc.
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2017-04-27
Decision date: 2017-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo Grove, IL, 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.