Aspen Laser Systems Therapy Laser System— 510(k) K150138

Name: FDA 510(k) clearance K150138
Creator: U.S. Food and Drug Administration
Published: 2015-05-08

Substantially Equivalent

Aspen Laser Systems, LLC

FDA 510(k) clearance K150138 for Aspen Laser Systems Therapy Laser System, Substantially Equivalent on 2015-05-08. Applicant: Aspen Laser Systems, LLC. Device class: 2.

Clearance details

Applicant: Aspen Laser Systems, LLC
Product code: Code PDZ
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2015-01-22
Decision date: 2015-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Reno, NV, US

Download summary PDF View on FDA.gov ↗

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