510(k) K896834 ยท GWM Device, Monitoring, Intracranial Pressure
MODEL BT-1 FOT BOLT INSTALLATION KIT
| Applicant | Pearl Instruments Corp., Highland Park IL, US |
| Decision | Substantially Equivalent, Feb 23, 1990 |
| Received | Dec 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896834
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.