510(k) K020764 ยท HAW Neurological Stereotaxic Instrument
NAVIPRO
| Applicant | Kinamed, Inc., Camarillo CA, US |
| Decision | Substantially Equivalent, Jun 3, 2002 |
| Received | Mar 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020764
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.