510(k) K822066 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA PNEUMOPHILA
| Applicant | Biodan Medical Systems, Ltd., Israel, IL |
| Decision | Substantially Equivalent, Sep 21, 1982 |
| Received | Jul 14, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822066
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.