510(k) K984059 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ANGIOCATH AUTOGUARD CATHETER, INSYTE AUTOGUARD CATHETER
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US |
| Decision | Substantially Equivalent, Apr 9, 1999 |
| Received | Nov 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984059
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.