510(k) K772063 ยท GWM Device, Monitoring, Intracranial Pressure
CATHETER, INTRACRANIAL PRESS. MONITOR.
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 3, 1978 |
| Received | Nov 2, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772063
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.