510(k) K883518 ยท GWM Device, Monitoring, Intracranial Pressure
EVENT MARKER & A SECOND PRESSURE TREND OUTPUT
| Applicant | Metatech Corp., Wheeling IL, US |
| Decision | Substantially Equivalent, Sep 22, 1988 |
| Received | Aug 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883518
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.