510(k) K101133 ยท GWM Device, Monitoring, Intracranial Pressure
SENSOMETRICS SOFTWARE
| Applicant | Dpcom AS, Ne MN, US |
| Decision | Substantially Equivalent, Nov 18, 2010 |
| Received | Apr 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101133
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.