510(k) K072379 ยท GWM Device, Monitoring, Intracranial Pressure
MPS OXIPORT AND MPS OXIPORT PLUS
| Applicant | Innerspace, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Apr 29, 2008 |
| Received | Aug 24, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072379
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.