510(k) K904013 ยท FPA Set, Administration, Intravascular
SPIVE NEEDLE SYSTEM, MODIFICATION
| Applicant | Pascall Medical Corp., Bethesda MD, US |
| Decision | Substantially Equivalent, Oct 1, 1990 |
| Received | Aug 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904013
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.