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FDA 510(k) Application Details - K152139
Device Classification Name
Transmitters And Receivers, Physiological Signal, Radiofrequency
More FDA Info for this Device
510(K) Number
K152139
Device Name
Transmitters And Receivers, Physiological Signal, Radiofrequency
Applicant
VITAL CONNECT, INC.
900 E. HAMILTON AVENUE, SUITE 500
CAMPBELL, CA 95008 US
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Contact
BONNIE WU
Other 510(k) Applications for this Contact
Regulation Number
870.2910
More FDA Info for this Regulation Number
Classification Product Code
DRG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/03/2015
Decision Date
12/06/2015
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
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