510(k) K890468 ยท GWM Device, Monitoring, Intracranial Pressure
MODEL FT-100 INTRACRANIAL PRESSURE MONITOR
| Applicant | Pearl Instruments Corp., Highland Park IL, US |
| Decision | Substantially Equivalent, Apr 26, 1989 |
| Received | Jan 31, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890468
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.