CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)— 510(k) K080300

Name: FDA 510(k) clearance K080300
Creator: U.S. Food and Drug Administration
Published: 2008-04-08

Substantially Equivalent

Cutera, Inc.

FDA 510(k) clearance K080300 for CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD), Substantially Equivalent on 2008-04-08. Applicant: Cutera, Inc.. Device class: 2.

Clearance details

Applicant: Cutera, Inc.
Product code: Code NUV
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2008-02-05
Decision date: 2008-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brisbane, CA, 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.