FDA 510(k) Applications Submitted by Alcresta Therapeutics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K243284 10/17/2024 RELiZORB (100300/ 100301) Alcresta Therapeutics, Inc.
K191379 05/23/2019 RELiZORB Alcresta Therapeutics, Inc.
K231156 04/24/2023 Enzyme Packed Cartridge - RELiZORB Alcresta Therapeutics, Inc.
K232784 09/11/2023 RELiZORB« Alcresta Therapeutics, Inc.
K161247 05/03/2016 Relizorb Alcresta Therapeutics, Inc.
K163057 11/01/2016 Relizorb Alcresta Therapeutics, Inc.


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