FDA 510(k) Application Details - K122333

Device Classification Name	Transmitters And Receivers, Physiological Signal, Radiofrequency   More FDA Info for this Device
510(K) Number	K122333
Device Name	Transmitters And Receivers, Physiological Signal, Radiofrequency
Applicant	AFRAME DIGITAL, INC. 1889 PRESTON WHITE DR STE 101 Reston, VA 20191 US Other 510(k) Applications for this Company
Contact	JILL THORPE 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	08/02/2012
Decision Date	11/19/2012
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