Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K052943 |
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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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ddR Formula B X-ray System, ddR Formula B Product Usage: X-ray system used for imaging | 2 | 09/25/2018 | Swissray Medical |
ddR Formula B X-ray System, Model ddR Formula B X-ray system used for imaging | 2 | 09/18/2018 | Swissray Medical |
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