510(k) K970255 ยท FPA Set, Administration, Intravascular
KIPP MED I.V. MANIFOLD
| Applicant | The Kipp Group, Ontario CA, US |
| Decision | Substantially Equivalent, Apr 14, 1997 |
| Received | Jan 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970255
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.