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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K000729
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8 FR 40CC Rediguard IAB, IAB-S840C, Intra-aortic balloon catheter. The Intra-aortic balloon (IAB... 1 04/16/2009 Arrow International, Inc.
9 FR 50CC Rediguard IAB, IAB-R950-U, Intra-aortic balloon catheter. The Intra-aortic balloon (IA... 1 04/16/2009 Arrow International, Inc.
ARROW 40cc Drive Line Kits, REF IAK-02692, Intra-aortic balloon catheter. The Intra-aortic ball... 1 04/16/2009 Arrow International, Inc.
Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 30 cc; Product Number:... 2 04/06/2013 Arrow International Inc
Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 40 cc; Product Number: ... 2 04/06/2013 Arrow International Inc
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