510(k) K955732 ยท FPA Set, Administration, Intravascular
VENTED SOLUTION SET
| Applicant | Distronic Sterile Products, Inc., Portsmouth NH, US |
| Decision | Substantially Equivalent, Feb 21, 1996 |
| Received | Dec 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955732
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.