FDA 510(k) Applications for Medical Device Product Code "PLQ"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K250499 | Alcresta Therapeutics, Inc | RELiZORB (100300/100301) | 04/17/2025 |
| K231156 | Alcresta Therapeutics, Inc. | Enzyme Packed Cartridge - RELiZORB | 08/30/2023 |
| K163057 | Alcresta Therapeutics, Inc. | Relizorb | 07/12/2017 |
| K191379 | Alcresta Therapeutics, Inc. | RELiZORB | 12/04/2019 |
| K161247 | Alcresta Therapeutics, Inc. | Relizorb | 06/30/2016 |
| K243284 | Alcresta Therapeutics, Inc. | RELiZORB (100300/ 100301) | 01/15/2025 |
| K232784 | Alcresta Therapeutics, Inc. | RELiZORB« | 12/21/2023 |
| DEN150001 | ALCRESTA, INC. | RELIZORB | 11/20/2015 |
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