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Luminex Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133302FLEXMAP 3DJanuary 10, 2014
K121399LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KJanuary 9, 2013
K073506LUMINEX LX 100/200 INSTRUMENTMarch 7, 2008