510(k) K042322 ยท FJD Detector, Leak, Blood
STERICHEK BLOOD LEAK REAGENT STRIPS
| Applicant | Hach Company, Elkhart IN, US |
| Decision | Substantially Equivalent, Dec 7, 2004 |
| Received | Aug 26, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042322
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.