510(k) K073436 ยท GEX Powered Laser Surgical Instrument
SPECTRA VRMII 1-SWITCHED ND:YAG LASER SYSTEM
| Applicant | Lutronic Corporation, North Reading MA, US |
| Decision | Substantially Equivalent, Dec 28, 2007 |
| Received | Dec 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073436
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.