510(k) K101712 ยท GEX Powered Laser Surgical Instrument
ENDOVASCULAR LAER VEIN SYSTEM KIT
| Applicant | Biolitec, Inc., Grandville MA, US |
| Decision | Substantially Equivalent, Oct 27, 2010 |
| Received | Jun 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101712
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.