510(k) K860290 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
VIAPIC CENTRAL LINE CATHETER
| Applicant | Parke-Davis Co., Rochester MI, US |
| Decision | Substantially Equivalent, Mar 18, 1986 |
| Received | Jan 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860290
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.