510(k) K083378 ยท GWM Device, Monitoring, Intracranial Pressure
SYNERGY
| Applicant | Innerspace, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Sep 29, 2009 |
| Received | Nov 14, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083378
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.