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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 42 Results
510(K) Number: K141979
 
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AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular and neurovascular imaging... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper F010/10 DRTable, System Code 722019 Vascular, cardiovascular and neurovascular imagi... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper F020 Biplane DR Table, System Code 722020 Vascular, cardiovascular and neurovascular... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper F020 DR Table, System Code 722015 Vascular, cardiovascular and neurovascular imaging... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper F010 DR Table, System Code 722014 Vascular, cardiovascular and neurovascular imaging... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper F020 DR Table, System Code 722023 Vascular, cardiovascular and neurovascular imaging... 2 09/21/2018 Philips Electronics North America Corporation
Allura Xper systems with Certeray X-ray Generator located in regions with high mains (480V) voltage.... 2 02/24/2018 Philips Electronics North America Corporation
Allura Xper FD and and Xper FD ORT - Philips X-ray Systems Product Usage: The Allura Xper FD10 a... 2 02/24/2018 Philips Electronics North America Corporation
Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD... 2 04/14/2017 Philips Electronics North America Corporation
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper ... 2 08/26/2016 Philips Electronics North America Corporation
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