Last synced on 14 November 2025 at 11:06 pm

RELiZORB (100300/100301)

Page Type
Cleared 510(K)
510(k) Number
K250499
510(k) Type
Traditional
Applicant
Alcresta Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2025
Days to Decision
56 days
Submission Type
Summary

RELiZORB (100300/100301)

Page Type
Cleared 510(K)
510(k) Number
K250499
510(k) Type
Traditional
Applicant
Alcresta Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2025
Days to Decision
56 days
Submission Type
Summary