FDA 510(k) Application Details - K033681

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K033681
Device Name	Introducer, Catheter
Applicant	TERUMO CORP. 125 BLUE BALL RD. ELKTON, MD 21921 US Other 510(k) Applications for this Company
Contact	MARK UNTERREINER 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	11/24/2003
Decision Date	12/11/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review