510(k) K890089 ยท LQF Dna-Reagents, Mycobacterium Spp.
RAPID DIAG. SYSTEM FOR MYCOBACTERIUM GORDONAE
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 13, 1989 |
| Received | Jan 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890089
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.