MICROLIGHT 830 LASER SYSTEM— 510(k) K010175
Substantially EquivalentMicrolight Corporation of America
FDA 510(k) clearance K010175 for MICROLIGHT 830 LASER SYSTEM, Substantially Equivalent on 2002-02-06. Applicant: Microlight Corporation of America.
Clearance details
- Applicant
- Microlight Corporation of America
- Product code
- Code NHN
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Missouri City, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.