510(k) K981683 ยท FPA Set, Administration, Intravascular
HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y
| Applicant | Venusa , Ltd., El Paso TX, US |
| Decision | Substantially Equivalent, Jul 28, 1998 |
| Received | May 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981683
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.