MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM— 510(k) K101147

Name: FDA 510(k) clearance K101147
Creator: U.S. Food and Drug Administration
Published: 2011-01-21

Substantially Equivalent

Alma Lasers, Inc.

FDA 510(k) clearance K101147 for MODIFIED ALMA LASERS FAMILY OF ACCENT RADIOFREQUENCY (RF) SYSTEM, Substantially Equivalent on 2011-01-21. Applicant: Alma Lasers, Inc.. Device class: 2.

Clearance details

Applicant: Alma Lasers, Inc.
Product code: Code NUV
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2010-04-23
Decision date: 2011-01-21
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.