510(k) K050702 ยท GWM Device, Monitoring, Intracranial Pressure
NEUROSYSTEMS 1TM MONITOR
| Applicant | Neurosystems, LLC, Woodstock VT, US |
| Decision | Substantially Equivalent, May 17, 2005 |
| Received | Mar 18, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050702
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.