FDA 510(k) Application Details - K972511

Device Classification Name	Catheter, Embolectomy   More FDA Info for this Device
510(K) Number	K972511
Device Name	Catheter, Embolectomy
Applicant	MICROVENA CORP. 1861 BUERKLE RD. WHITE BEAR LAKE, MN 55110-5426 US Other 510(k) Applications for this Company
Contact	JANELL COLLEY Other 510(k) Applications for this Contact
Regulation Number	870.5150   More FDA Info for this Regulation Number
Classification Product Code	DXE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/03/1997
Decision Date	03/06/1998
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