510(k) K982702 ยท GWM Device, Monitoring, Intracranial Pressure
VENTRIX SUBDURAL TUNNELING PRESSURE MONITORING KIT MODEL NL950-SD
| Applicant | Camino Neurocare, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 10, 1998 |
| Received | Aug 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982702
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.