FDA 510(k) Application Details - K980487

Device Classification Name	Ring, Annuloplasty   More FDA Info for this Device
510(K) Number	K980487
Device Name	Ring, Annuloplasty
Applicant	BAXTER EDWARDS 17221 RED HILL AVE. IRVINE, CA 92614-5627 US Other 510(k) Applications for this Company
Contact	LARRY WOOD Other 510(k) Applications for this Contact
Regulation Number	870.3800   More FDA Info for this Regulation Number
Classification Product Code	KRH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/09/1998
Decision Date	07/07/1998
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