510(k) K002392 ยท GWM Device, Monitoring, Intracranial Pressure
VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-V
| Applicant | Integra Neurocare, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 2, 2000 |
| Received | Aug 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002392
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.