510(k) K171666 ยท GWM Device, Monitoring, Intracranial Pressure
MPR2 logO DATALOGGER
| Applicant | Raumedic AG, Helmbrechts, DE |
| Decision | Substantially Equivalent, Jul 6, 2017 |
| Received | Jun 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171666
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.