510(k) K000805 ยท GEX Powered Laser Surgical Instrument
KAVO K.E.Y. LASER 1242
| Applicant | Kavo America, Lake Zurich IL, US |
| Decision | Substantially Equivalent, May 4, 2000 |
| Received | Mar 13, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000805
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.