Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K182076 |
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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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Elekta Unity | 2 | 01/09/2019 | Elekta Limited |
Elekta Unity, Image-Guided Radiation Therapy System Product Usage: Elekta Unity using Magnetic R... | 2 | 04/08/2019 | Elekta Limited |
Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated f... | 2 | 05/08/2019 | Elekta Limited |
Elekta Unity, Image-Guided Radiation Therapy System Elekta Unity using Magnetic Resonance Imaging... | 2 | 07/16/2019 | Elekta, Inc. |
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