ACCULASER PRO4— 510(k) K023060

Substantially Equivalent

Acculaser, Inc.

FDA 510(k) clearance K023060 for ACCULASER PRO4, Substantially Equivalent on 2004-03-19. 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: 2002-09-13
Decision date: 2004-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chevy Chase, MD, 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.