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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
510(K) Number: K071923
 
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FLIXENE, 6X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
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