FDA 510(k) Application Details - K970528

Device Classification Name	Wire, Guide, Catheter   More FDA Info for this Device
510(K) Number	K970528
Device Name	Wire, Guide, Catheter
Applicant	SCHNEIDER (EUROPE) GMBH ACKERSTRASSE 6 BULACH CH-8180 CH Other 510(k) Applications for this Company
Contact	RUDOLF OTT Other 510(k) Applications for this Contact
Regulation Number	870.1330   More FDA Info for this Regulation Number
Classification Product Code	DQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/11/1997
Decision Date	06/10/1997
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