510(k) K082096 ยท GEX Powered Laser Surgical Instrument
POWERLIPO LASER SYSTEM
| Applicant | Lutronic Corporation, North Reading MA, US |
| Decision | Substantially Equivalent, Oct 8, 2008 |
| Received | Jul 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082096
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.