FDA 510(k) Application Details - K130750

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K130750
Device Name	Computer, Diagnostic, Programmable
Applicant	RHYTHMIA MEDICAL, INC 111 SOUTH BEDFORD ST SUITE 205 BURLINGTON, MA 01803 US Other 510(k) Applications for this Company
Contact	LEON AMARIGLIO Other 510(k) Applications for this Contact
Regulation Number	870.1425   More FDA Info for this Regulation Number
Classification Product Code	DQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2013
Decision Date	07/22/2013
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