FDA 510(k) Applications Submitted by LUMINEX CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133302 | 10/25/2013 | FLEXMAP 3D | LUMINEX CORP. |
| K073506 | 12/13/2007 | LUMINEX LX 100/200 INSTRUMENT | LUMINEX CORP. |
| K121399 | 05/09/2012 | LUMINEX FLEXMAP 3D INSTRUMENT SYSTEM, LUMINEX XPONENT 4.0 SPI SOFTWARE, FLEXMAP 3D IVD CALIBRATION KIT, FLEXMAP 3D IVD P | LUMINEX CORP. |
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