510(k) K984298 ยท HAW Neurological Stereotaxic Instrument
Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI
| Applicant | Z-Kat, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Jun 23, 1999 |
| Received | Dec 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984298
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.