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FDA 510(k) Applications Submitted by CARDIO-PHOENIX INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K182790
10/01/2018
Cardio-TriTest v6.5
Cardio-Phoenix Inc.
K143432
12/01/2014
Cardio-TriTest
CARDIO-PHOENIX INC.
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