Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K133580 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600... | 2 | 10/27/2020 | Siemens Medical Solutions USA, Inc |
Artis oneFloor-mounted system for uncompromised imaging; Artis one, Interventional fluoroscopic x-ra... | 2 | 02/14/2018 | Siemens Medical Solutions USA, INC |
Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system develo... | 2 | 03/20/2018 | Siemens Medical Solutions USA, Inc |
Artis One; The Artis One is an angiography system developed for diagnostic interventional procedures... | 2 | 02/17/2015 | Siemens Medical Solutions USA, Inc |
Artis One, Interventional, Fluoroscopic, x-ray system Artis one is an angiography system developed ... | 2 | 03/31/2016 | Siemens Medical Solutions USA, Inc |
ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventi... | 2 | 04/27/2023 | Siemens Medical Solutions USA, Inc |
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