510(k) K003747 ยท DBA Complement C1 Inhibitor (Inactivator), Antigen, Antiserum, Control
C1-INHIBITOR MICROTITER ASSAY DEVICE
| Applicant | Baxter Healthcare Corp, Glendale CA, US |
| Decision | Substantially Equivalent, Mar 19, 2001 |
| Received | Dec 4, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003747
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.