510(k) K033861 ยท LQH Dna-Reagents, Legionella
BD PROBETEC ET LEGIONELLA PNEUMOPHILA (LP) AMPLIFIED DNA ASSAY
| Applicant | Becton, Dickinson & CO, Sparks MD, US |
| Decision | Substantially Equivalent, Mar 9, 2004 |
| Received | Dec 12, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033861
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.