510(k) K152670 ยท GWM Device, Monitoring, Intracranial Pressure
DirectLink ICP Module, DirectLink ICP Extension Cable, Patient Monitor Interface Cables
| Applicant | Medos International SARL, Le Locle, CH |
| Decision | Substantially Equivalent, Jan 22, 2016 |
| Received | Sep 17, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152670
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.