510(k) K840003 ยท GWM Device, Monitoring, Intracranial Pressure
DISPOSABLE ICP KIT DIFF. SIZES
| Applicant | Codman & Shurtleff, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 28, 1984 |
| Received | Jan 4, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840003
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.