510(k) K812006 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA DIRECT FLUORESCENT ANTIBODY
| Applicant | Centers for Disease Control and Prevention, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 8, 1981 |
| Received | Jul 16, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812006
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.