AXIOM BIOLASER LLLT SERIES-3— 510(k) K033015

Substantially Equivalent

Axiom Usa., Inc.

FDA 510(k) clearance K033015 for AXIOM BIOLASER LLLT SERIES-3, Substantially Equivalent on 2003-11-25. Applicant: Axiom Usa., Inc..

Clearance details

Applicant
Axiom Usa., Inc.
Product code
Code NHN
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Tampa, FL, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.