Q-CLEAR— 510(k) K110370

Substantially Equivalent

Light Age, Inc.

FDA 510(k) clearance K110370 for Q-CLEAR, Substantially Equivalent on 2011-09-15. Applicant: Light Age, Inc.. Device class: 2.

Clearance details

Applicant: Light Age, Inc.
Product code: Code PDZ
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2011-02-08
Decision date: 2011-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, NJ, 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.