FDA 510(k) Application Details - K110878

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K110878
Device Name	Computer, Diagnostic, Programmable
Applicant	TOPERA, INC. 11445 E. VIA LINDA SUITE 2, P.O. BOX 224 SCOTTSDALE, AZ 85259 US Other 510(k) Applications for this Company
Contact	RUCHIR SEHRA 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	03/30/2011
Decision Date	09/23/2011
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