510(k) K014113 ยท HAW Neurological Stereotaxic Instrument
ENDOMAP
| Applicant | Siemens Medical Solutions USA, Inc., Iselin NJ, US |
| Decision | Substantially Equivalent, Jun 14, 2002 |
| Received | Dec 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014113
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.