FDA 510(k) Applications for Medical Device Product Code "PFA"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K151776 | Mespere LifeSciences Inc. | Central Venous Pressure System | 08/12/2015 |
| K131085 | MESPERE LIFESCIENCES INC. | CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000 | 08/22/2013 |
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