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

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..

Clearance details

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

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