510(k) K950597 ยท FPA Set, Administration, Intravascular
CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE
| Applicant | Distronic Sterile Products, Inc., Portsmouth NH, US |
| Decision | Substantially Equivalent, Jul 26, 1995 |
| Received | Feb 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950597
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.