510(k) K020558 ยท GWM Device, Monitoring, Intracranial Pressure
LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE
| Applicant | Integra Neurosciences, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 21, 2002 |
| Received | Feb 20, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020558
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.