510(k) K983963 ยท GEX Powered Laser Surgical Instrument
DORNIER MEDILA H
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Nov 25, 1998 |
| Received | Nov 6, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983963
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.