510(k) K911771 ยท LJK Antisera, If, Toxoplasma Gondii
ARD(TM) ANTIMICROBIAL REMOVAL DEVICE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Jul 1, 1991 |
| Received | Apr 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911771
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.