Luminex Corp. - FDA 510(k) Cleared Devices
Recent clearances: FLEXMAP 3D, LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P, LUMINEX LX 100/200 INSTRUMENT
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Luminex Corp. Pathology ✕
1 devices