FDA 510(k) Applications for Medical Device Product Code "OUS"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K120563 | MICROPHAGE, INC. | KEYPATH MRSA/MSSA BLOOD CULTURE TEST-BT | 03/30/2012 |
| K102342 | MICROPHAGE, INC. | KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT | 05/05/2011 |
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