510(k) K862820 ยท GWM Device, Monitoring, Intracranial Pressure
LADD/STERITEK ICP MONITOR, CAT. NO. P3000
| Applicant | Ladd Research Industries, Inc., Burlington VT, US |
| Decision | Substantially Equivalent, Feb 26, 1987 |
| Received | Jul 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862820
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.