510(k) K871795 ยท LQF Dna-Reagents, Mycobacterium Spp.
RAPID DIAGNOSTIC SYSTEM FOR MYCOBACTERIUM TUBER.
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 30, 1987 |
| Received | May 7, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871795
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.