510(k) K860574 ยท LQG Dna-Reagents, Mycoplasma Spp.
GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 3, 1986 |
| Received | Feb 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860574
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.