510(k) K822636 ยท GWM Device, Monitoring, Intracranial Pressure
CLASS II DEVICE FOR I.C.P. MONITORING
| Applicant | Philadelphia Medical Specialties, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 14, 1982 |
| Received | Aug 31, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822636
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.