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FDA 510(k) Application Details - K242552
Device Classification Name
System, Image Processing, Radiological
More FDA Info for this Device
510(K) Number
K242552
Device Name
System, Image Processing, Radiological
Applicant
iCat Solutions Ltd
51-59 Rose Lane
Norwich NR1 1BY GB
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Contact
Georgios Michalopoulos
Other 510(k) Applications for this Contact
Regulation Number
892.2050
More FDA Info for this Regulation Number
Classification Product Code
LLZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/27/2024
Decision Date
04/08/2025
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K242552
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