510(k) K041838 ยท GWM Device, Monitoring, Intracranial Pressure
MPS (OR MPS-T)
| Applicant | Innerspace, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Mar 1, 2005 |
| Received | Jul 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041838
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.