510(k) K852237 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA IMMUNOFLUORESCENT ANTIBODY TEST KIT
| Applicant | Genetic Systems Corp., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 22, 1985 |
| Received | May 22, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852237
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.