510(k) K120252 ยท GWM Device, Monitoring, Intracranial Pressure
RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM
| Applicant | Raumedic AG, Helmbrechts, DE |
| Decision | Substantially Equivalent, Apr 11, 2012 |
| Received | Jan 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120252
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.