510(k) K112017 ยท GWM Device, Monitoring, Intracranial Pressure
RAUMEDIC ICP MONITORING SYSTEM
| Applicant | Raumedic AG, Helmbrechts, DE |
| Decision | Substantially Equivalent, Oct 11, 2011 |
| Received | Jul 14, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112017
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.