510(k) K130529 ยท GWM Device, Monitoring, Intracranial Pressure
RAUMEDIC-PTO-MONITORING-SYSTEM
| Applicant | Raumedic AG, Helmbrechts, DE |
| Decision | Substantially Equivalent, Oct 25, 2013 |
| Received | Mar 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130529
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.