FDA 510(k) Application Details - K102948

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K102948
Device Name	Introducer, Catheter
Applicant	BAYLIS MEDICAL CO., INC. 2645 MATHESON BLVD. E MISSISSAUGA, ONTARIO L4W 5S4 CA Other 510(k) Applications for this Company
Contact	MEGHAL KHAKHAR 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	10/05/2010
Decision Date	04/01/2011
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