510(k) K862012 ยท GWM Device, Monitoring, Intracranial Pressure
LADD MEDICAL S-2000
| Applicant | Ladd Research Industries, Inc., Burlington VT, US |
| Decision | Substantially Equivalent, Jun 9, 1986 |
| Received | May 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862012
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.