510(k) K161010 ยท GWM Device, Monitoring, Intracranial Pressure
HICP200 Patient/Monitor Interconnect Cable
| Applicant | Innerspace Neuro Solutions, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Oct 20, 2016 |
| Received | Apr 11, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161010
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.