FDA 510(k) Application Details - K180081

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K180081
Device Name	Introducer, Catheter
Applicant	Cordis Corporation 1820 McCarthy Boulevard Milpitas, CA 95035 US Other 510(k) Applications for this Company
Contact	Michelle Ragozzino Rodgers Other 510(k) Applications for this Contact
Regulation Number	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/11/2018
Decision Date	04/18/2018
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