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FDA 510(k) Application Details - K241633
Device Classification Name
More FDA Info for this Device
510(K) Number
K241633
Device Name
Informed Vital Core Application (IVC App)
Applicant
Mindset Medical, Inc.
12439 N 32nd St.
Phoenix, AZ 85032 US
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Contact
Chris Joslin
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Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
QME
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More FDA Info for this Product Code
Date Received
06/06/2024
Decision Date
11/18/2024
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 K241633
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