510(k) K893395 ยท GWM Device, Monitoring, Intracranial Pressure
MINI-MONITOR J7000 ICP
| Applicant | Ladd Research Industries, Inc., Burlington VT, US |
| Decision | Substantially Equivalent, Nov 22, 1989 |
| Received | May 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893395
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.