510(k) K830820 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA DFA KIT I
| Applicant | Bionetic Laboratory Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 8, 1983 |
| Received | Mar 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830820
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.