510(k) K881183 ยท GWM Device, Monitoring, Intracranial Pressure
VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H
| Applicant | Camino Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, May 4, 1988 |
| Received | Mar 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881183
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.