510(k) K090164 ยท GEX Powered Laser Surgical Instrument
CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER
| Applicant | Biolitec, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 26, 2009 |
| Received | Jan 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090164
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.