Last synced on 14 November 2025 at 11:06 pm

Relizorb

Page Type
Cleared 510(K)
510(k) Number
K161247
510(k) Type
Traditional
Applicant
Alcresta Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2016
Days to Decision
58 days
Submission Type
Summary

Relizorb

Page Type
Cleared 510(K)
510(k) Number
K161247
510(k) Type
Traditional
Applicant
Alcresta Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2016
Days to Decision
58 days
Submission Type
Summary