• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K132447, VITALCONNECT PLATFORM BY VITAL CONNECT INC., by Vitalconnect, Inc.

FDA 510(k) K132447, VITALCONNECT PLATFORM BY VITAL CONNECT INC., by Vitalconnect, Inc.

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510(K) Number: K132447
Device Name: VITALCONNECT PLATFORM BY VITAL CONNECT INC.
Manufacturer: Vitalconnect, Inc.
Device Classification Name: Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation Number: DRG
Classification Product Code: KXA
Date Received: 08/06/2013
Decision Date: 04/03/2014
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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