510(k) K133302 ยท NSU Instrumentation For Clinical Multiplex Test Systems
FLEXMAP 3D
| Applicant | Luminex Corp., Austin TX, US |
| Decision | Substantially Equivalent, Jan 10, 2014 |
| Received | Oct 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133302
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.