ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE— 510(k) K020657

Name: FDA 510(k) clearance K020657
Creator: U.S. Food and Drug Administration
Published: 2002-07-29

Substantially Equivalent

Acculaser, Inc.

FDA 510(k) clearance K020657 for ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE, Substantially Equivalent on 2002-07-29. Applicant: Acculaser, Inc.. Device class: 2.

Clearance details

Applicant: Acculaser, Inc.
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2002-02-28
Decision date: 2002-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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