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FDA 510(k) Applications Submitted by Alcresta Therapeutics, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191379
05/23/2019
RELiZORB
Alcresta Therapeutics, Inc.
K231156
04/24/2023
Enzyme Packed Cartridge - RELiZORB
Alcresta Therapeutics, Inc.
K161247
05/03/2016
Relizorb
Alcresta Therapeutics, Inc.
K163057
11/01/2016
Relizorb
Alcresta Therapeutics, Inc.
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