510(k) K080248 ยท GEX Powered Laser Surgical Instrument
SPECTRA VRMIII Q-SWITCHED ND: YAG LASER SYSTEM AND DYE HANDPIECES
| Applicant | Lutronic Corporation, North Reading MA, US |
| Decision | Substantially Equivalent, Apr 23, 2008 |
| Received | Jan 31, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080248
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.