FDA 510(k) Application Details - K982538

Device Classification Name	System, Balloon, Intra-Aortic And Control   More FDA Info for this Device
510(K) Number	K982538
Device Name	System, Balloon, Intra-Aortic And Control
Applicant	BELMONT INSTRUMENT CORP. 780 BOSTON RD. BILLERICA, MA 01821 US Other 510(k) Applications for this Company
Contact	URAIWAN P LABADINI Other 510(k) Applications for this Contact
Regulation Number	870.3535   More FDA Info for this Regulation Number
Classification Product Code	DSP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/21/1998
Decision Date	10/02/1998
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