FDA 510(k) Applications for Medical Device Product Code "PTD"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K163001 | C.R. BARD, INC. | PowerFlow Apheresis I.V. Port | 04/17/2017 |
| K191143 | C.R. Bard, Inc. | PowerFlow Implantable Apheresis IV Port | 08/02/2019 |
| K192291 | Norfolk Medical Products, Inc. | TidalPort-AP Implantable Apheresis Vascular Access Port | 08/20/2020 |
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