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FDA 510(k) Applications Submitted by FEops nv
FDA 510(k) Number
Submission Date
Device Name
Applicant
K223855
12/23/2022
FEops HEARTguideTM, FEops HEARTguideTM ALPACA
FEops nv
K214066
12/27/2021
FEops HEARTguide
FEops nv
DEN200030
05/07/2020
FEops HEARTguide
FEops NV
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