510(k) K802100 ยท GWM Device, Monitoring, Intracranial Pressure
INTRACRANIAL PRESSURING MONITORING SYST.
| Applicant | Pudenz-Schulte Medical Research Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 16, 1980 |
| Received | Sep 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802100
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.