510(k) K022638 ยท GWM Device, Monitoring, Intracranial Pressure
NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT
| Applicant | Neurorecovery, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Oct 31, 2002 |
| Received | Aug 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022638
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.