510(k) K010175 ยท NHN Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
MICROLIGHT 830 LASER SYSTEM
| Applicant | Microlight Corporation of America, Missouri City TX, US |
| Decision | Substantially Equivalent, Feb 6, 2002 |
| Received | Jan 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010175
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.