Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K192482 |
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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, Image-Guided Radiation Therapy System | 2 | 06/30/2020 | Elekta, Inc. |
Elekta Unity, Philips Marlin Software versions: R5.3.30, R5.3.31, R6.0.5331, R5.7.0, R5.7.1, R6.1.57... | 2 | 06/08/2020 | Elekta Limited |
Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: is indicate... | 2 | 06/05/2020 | Elekta, Inc. |
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