FDA 510(k) Application Details - K112559

Device Classification Name	Transmitters And Receivers, Physiological Signal, Radiofrequency   More FDA Info for this Device
510(K) Number	K112559
Device Name	Transmitters And Receivers, Physiological Signal, Radiofrequency
Applicant	MEDAPPS, INC. 7975 NORTH HAYDEN ROAD SUITE A-203 SCOTTSDALE, AZ 85258 US Other 510(k) Applications for this Company
Contact	KENT DICKS 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	09/02/2011
Decision Date	12/02/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review