510(k) K860498 ยท LQH Dna-Reagents, Legionella
GEN-PROBE LEGIONELLA RAPID DIAGNOSTIC SYSTEM
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 16, 1986 |
| Received | Feb 10, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860498
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.