FDA 510(k) Application Details - K180722

Device Classification Name	More FDA Info for this Device
510(K) Number	K180722
Device Name	CAPERE Thrombectomy System
Applicant	KP Medcure, Inc. 1500 S. Sunkist Street, Suite H Anaheim, CA 92806 US Other 510(k) Applications for this Company
Contact	Samuel Shaolian Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QEW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2018
Decision Date	06/11/2018
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