510(k) K890422 ยท GHH Fibrin Split Products
ABBOTT TESTPACK(TM) D-DIMER
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Mar 27, 1989 |
| Received | Jan 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890422
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.