510(k) DEN200043 ยท QMV Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness
FilmArray Global Fever Panel
| Applicant | Biofire Defense, LLC, Salt Lake City UT, US |
| Decision | Unknown, Nov 20, 2020 |
| Received | Jun 26, 2020 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN200043
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.