510(k) K961858 ยท HAW Neurological Stereotaxic Instrument
COSGROVE DEPTH ELECTRODE KIT(CDEK)
| Applicant | Radionics, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Aug 7, 1996 |
| Received | May 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961858
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.