510(k) K000152 ยท FPA Set, Administration, Intravascular
KIPPMED I.V. MANIFOLD
| Applicant | The Kipp Group, Ontario CA, US |
| Decision | Substantially Equivalent, Feb 29, 2000 |
| Received | Jan 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000152
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.