510(k) K813440 ยท GWM Device, Monitoring, Intracranial Pressure
PHILLY BOLT
| Applicant | Philadelphia Medical Specialties, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 18, 1981 |
| Received | Dec 8, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813440
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.