510(k) K121399 ยท NSU Instrumentation For Clinical Multiplex Test Systems
LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P
| Applicant | Luminex Corp., Austin TX, US |
| Decision | Substantially Equivalent, Jan 9, 2013 |
| Received | May 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121399
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.