AXIOM BIOLASER LLLT SERIES-3— 510(k) K033015
Substantially EquivalentAxiom 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.