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FDA 510(k) Application Details - K250932
Device Classification Name
Computer, Diagnostic, Programmable
More FDA Info for this Device
510(K) Number
K250932
Device Name
Computer, Diagnostic, Programmable
Applicant
Medicalgorithmics S.A.
Aleje Jerozolimskie 81
Warsaw 02-001 PL
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Contact
Agnieszka Romowicz
Other 510(k) Applications for this Contact
Regulation Number
870.1425
More FDA Info for this Regulation Number
Classification Product Code
DQK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/28/2025
Decision Date
05/27/2025
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K250932
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