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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