FDA 510(k) Applications Submitted by ROBERT GALLOTTO

FDA 510(k) Number Submission Date Device Name Applicant
DEN150001 01/02/2015 RELIZORB ALCRESTA, INC.
K161247 05/03/2016 Relizorb Alcresta Therapeutics, Inc.
K163057 11/01/2016 Relizorb Alcresta Therapeutics, Inc.


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