510(k) K821266 ยท GRP Antisera, All Types, H. Influenza
BBL DIRECTIGEN MENINGITIS TEST KIT
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Jun 1, 1982 |
| Received | May 3, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821266
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.