510(k) K901640 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MULTICATH PLACEMENT KIT
| Applicant | Vygon Corp., New York NY, US |
| Decision | Substantially Equivalent, Aug 10, 1990 |
| Received | Apr 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901640
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.