FDA 510(k) Application Details - K242437

Device Classification Name Analyzer,Medical Image

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510(K) Number K242437
Device Name Analyzer,Medical Image
Applicant Cube Click, Inc.
105 East 34 Street
Suite 231
New York, NY 10016 US
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Contact Richard Ricci
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Regulation Number 000.0000

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Classification Product Code MYN
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Date Received 08/16/2024
Decision Date 05/14/2025
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 K242437


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