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FDA 510(k) Applications Submitted by ROBERT T.V. KUNG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070225
01/24/2007
SUPRACOR INTR-AORTIC BALLOON PUMP CONSOLE
ABIOMED, INC.
K063723
12/15/2006
IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
ABIOMED, INC.
K062582
08/31/2006
SUPRACOR BALLOON CATHETER
ABIOMED, INC.
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