FDA 510(k) Applications for Medical Device Product Code "PUQ"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K170509 | Bio-Rad Laboratories | BioPlex 2200 ToRC IgM, BioPlex 2200 ToRC IgM Calibrator Set, BioPlex 2200 ToRC IgM Control Set | 05/19/2017 |
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