CUTERA GENESISPLUS LASER SYSTEM— 510(k) K103626

Substantially Equivalent

Cutera, Inc.

FDA 510(k) clearance K103626 for CUTERA GENESISPLUS LASER SYSTEM, Substantially Equivalent on 2011-04-05. Applicant: Cutera, Inc.. Device class: 2.

Clearance details

Applicant: Cutera, Inc.
Product code: Code PDZ
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2010-12-10
Decision date: 2011-04-05
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.