510(k) K921421 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY
| Applicant | Pro-Lab, Inc., Ontario Canada M5m 1c9, CA |
| Decision | Substantially Equivalent, Jul 28, 1992 |
| Received | Mar 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921421
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.