Alcresta Therapeutics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250499RELiZORB (100300/100301)April 17, 2025
K243284RELiZORB (100300/ 100301)January 15, 2025
K232784RELiZORB®December 21, 2023
K231156Enzyme Packed Cartridge - RELiZORBAugust 30, 2023
K191379RELiZORBDecember 4, 2019
K163057RelizorbJuly 12, 2017
K161247RelizorbJune 30, 2016