LUMINEX LL LASER SYSTEM— 510(k) K063574

Name: FDA 510(k) clearance K063574
Creator: U.S. Food and Drug Administration
Published: 2007-01-29

Substantially Equivalent

Medical Laser Systems, Inc.

FDA 510(k) clearance K063574 for LUMINEX LL LASER SYSTEM, Substantially Equivalent on 2007-01-29. Applicant: Medical Laser Systems, Inc.. Device class: 2.

Clearance details

Applicant: Medical Laser Systems, Inc.
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2006-11-29
Decision date: 2007-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wahington, DC, US

Download summary PDF View on FDA.gov ↗

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