510(k) K954983 ยท FPA Set, Administration, Intravascular
EXTENSION SET WITH CHECK VALVE
| Applicant | Distronic Sterile Products, Inc., Portsmouth NH, US |
| Decision | Substantially Equivalent, Jan 23, 1996 |
| Received | Oct 31, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954983
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.