510(k) K853864 ยท GWM Device, Monitoring, Intracranial Pressure
INTRACRANIAL PRESSURE MONITORING KIT 070
| Applicant | Camino Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 20, 1986 |
| Received | Sep 17, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853864
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.