FDA 510(k) Application Details - K133703

Device Classification Name	Transmitters And Receivers, Electrocardiograph, Telephone   More FDA Info for this Device
510(K) Number	K133703
Device Name	Transmitters And Receivers, Electrocardiograph, Telephone
Applicant	COMMWELL R&D LTD. 555 THIRTEENTH STREET NW WASHINGTON, DC 20004 US Other 510(k) Applications for this Company
Contact	JONATHON KAHAN Other 510(k) Applications for this Contact
Regulation Number	870.2920   More FDA Info for this Regulation Number
Classification Product Code	DXH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/03/2013
Decision Date	08/18/2014
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