510(k) K861510 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MULTILUMEN VIAPIC CENTRAL LINE CATHETER
| Applicant | Warner-Lambert Co., Sandy UT, US |
| Decision | Substantially Equivalent, Jun 9, 1986 |
| Received | Apr 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861510
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.