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FDA 510(k) Applications Submitted by RADLogics, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120161
01/19/2012
ALPHAPOINT IMAGING SOFTWARE
RADLOGICS, INC.
K193300
11/27/2019
AIMI-Triage CXR PTX
RADLogics, Inc.
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