CYNOSURE CELLULAZE LASER— 510(k) K102541

Substantially Equivalent

Cynosure, Inc.

FDA 510(k) clearance K102541 for CYNOSURE CELLULAZE LASER, Substantially Equivalent on 2012-01-26. Applicant: Cynosure, Inc.. Device class: 2.

Clearance details

Applicant: Cynosure, Inc.
Product code: Code OYW
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2010-09-03
Decision date: 2012-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wesford, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OYW

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Data sourced from openFDA. This site is unofficial and independent of the FDA.