FDA 510(k) Application Details - K172995

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K172995
Device Name	Introducer, Catheter
Applicant	Terumo Medical Corporation 950 Elkton Blvd Elkton, MD 21921 US Other 510(k) Applications for this Company
Contact	Liang Lu 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	09/27/2017
Decision Date	11/21/2017
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