510(k) K832896 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA INDIRECT FLUORESCENT ANTIBOD
| Applicant | Biodan Medical Systems, Ltd., Rehovot, Israel, US |
| Decision | Substantially Equivalent, Oct 14, 1983 |
| Received | Aug 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832896
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.