510(k) K910159 ยท FPA Set, Administration, Intravascular
WINGED ADMININ. SET W/NON-CORING NEEDLE
| Applicant | Dmd Products, San Carlos CA, US |
| Decision | Substantially Equivalent, Sep 6, 1991 |
| Received | Jan 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910159
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.