510(k) K960324 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control
HEMAGEN CRP 150 KIT (EIA METHOD)
| Applicant | Hemagen Diagnostics, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 12, 1996 |
| Received | Jan 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960324
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.