FDA 510(k) Application Details - K190749

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K190749
Device Name	Catheter, Percutaneous
Applicant	Q'Apel 330 Wilshire Boulevard Santa Monica, CA 90401 US Other 510(k) Applications for this Company
Contact	Ken Peartree Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/2019
Decision Date	07/15/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review