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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K173639
 
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LUMINOS Lotus Max (VF11) 2 05/23/2023 Siemens Medical Solutions USA, Inc
Luminos dRF Max (VE10, VF10, VF11) 2 05/23/2023 Siemens Medical Solutions USA, Inc
Luminos Agile Max (VE10, VF10, VF11) 2 05/23/2023 Siemens Medical Solutions USA, Inc
Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluor... 2 02/23/2023 Siemens Medical Solutions USA, Inc
Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fl... 2 02/23/2023 Siemens Medical Solutions USA, Inc
Luminos Agile Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluor... 2 02/23/2023 Siemens Medical Solutions USA, Inc
Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max 2 01/20/2023 Siemens Medical Solutions USA, Inc
Uroskop Omnia Max, Model no. 10762473 - Product Usage: a solid state detector fluoroscopic X-ray sys... 2 01/08/2021 Siemens Medical Solutions USA, Inc
SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage: is a device intended to vi... 2 08/05/2020 Siemens Medical Solutions USA, Inc
SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is a device intended to visua... 2 08/05/2020 Siemens Medical Solutions USA, Inc
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