510(k) K890409 ยท GGP Test, Qualitative And Quantitative Factor Deficiency
DADE(R) PLASMINOGEN CHROMOGENIC ASSAY
| Applicant | Baxter Healthcare Corp, Miami FL, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Jan 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890409
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.