510(k) K072262 ยท GEX Powered Laser Surgical Instrument
GENTLERAY 980 DIODE LASER SYSTEM
| Applicant | Kavo America, Lake Zurich IL, US |
| Decision | Substantially Equivalent, Oct 26, 2007 |
| Received | Aug 15, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072262
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.