510(k) DEN160033 ยท PUJ Voriconazole Test System
ARK Voriconazole II Assay Test System
| Applicant | Ark Diagnostics, Inc., Fremont CA, US |
| Decision | Unknown, May 5, 2017 |
| Received | Jul 15, 2016 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN160033
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.