510(k) K883881 ยท GWM Device, Monitoring, Intracranial Pressure
MODIFIED MODEL 2001 FIBER OPTICS CATHETER
| Applicant | Metatech Corp., Wheeling IL, US |
| Decision | Substantially Equivalent, Oct 27, 1988 |
| Received | Jul 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883881
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.