510(k) K854657 ยท GWM Device, Monitoring, Intracranial Pressure
INTRACRANIAL PRESSURE MONITORING CUP CATHETERS
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Dec 27, 1985 |
| Received | Nov 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854657
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.