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FDA 510(k) Applications Submitted by Ablacon, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230008
01/03/2023
Ablamap« System
Ablacon, Inc.
K203084
10/13/2020
Ablamap Software
Ablacon, Inc.
K223666
12/07/2022
AblacathÖ Mapping Catheter
Ablacon, Inc.
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