510(k) K103206 ยท GWM Device, Monitoring, Intracranial Pressure
RAUMEDIC- ICP-MONITORING SYSTEM
| Applicant | Raumedic AG, Helmbrechts, DE |
| Decision | Substantially Equivalent, Mar 4, 2011 |
| Received | Nov 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103206
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.