510(k) K981846 ยท GWM Device, Monitoring, Intracranial Pressure
PARENCHYMAL BOLT PRESSURE MONITORING KIT
| Applicant | Camino Neurocare, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 18, 1998 |
| Received | May 26, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981846
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.