510(k) K965024 ยท DBA Complement C1 Inhibitor (Inactivator), Antigen, Antiserum, Control
N-ASSAY TIA C1-INACTIVATOR TEST KIT
| Applicant | Crestat Diagnostics, Inc., Weston CT, US |
| Decision | Substantially Equivalent, Jul 14, 1997 |
| Received | Dec 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965024
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.