FDA 510(k) Applications for Medical Device Product Code "PFX"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| DEN130018 | Affymetrix, Inc. | CYTOSCAN(R) DX | 01/17/2014 |
| K163367 | Agilent Technologies, Inc. | GenetiSure Dx Postnatal Assay | 08/11/2017 |
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