510(k) K880154 ยท GWM Device, Monitoring, Intracranial Pressure
METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM
| Applicant | Metatech Corp., Wheeling IL, US |
| Decision | Substantially Equivalent, Mar 28, 1988 |
| Received | Jan 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880154
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.