510(k) K123805 ยท FJD Detector, Leak, Blood
E-Z CHEK BLOOD LEAK TEST STRIPS
| Applicant | Reprocessing Products Corp, Tucson AZ, US |
| Decision | Substantially Equivalent, Mar 20, 2013 |
| Received | Dec 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123805
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.