510(k) K070189 ยท FPA Set, Administration, Intravascular
ACCU-CHEK ULTRAFLEX INFUSION SET
| Applicant | Disetronic Medical Systems AG, Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 21, 2007 |
| Received | Jan 22, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070189
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.