510(k) K172209 ยท GWM Device, Monitoring, Intracranial Pressure
AURA ICP MONITORING SYSTEM
| Applicant | Branchpoint Technologies, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 18, 2018 |
| Received | Jul 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172209
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.