Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K180589 |
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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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AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product U... | 2 | 06/03/2020 | Agfa N.V. |
AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 8... | 2 | 07/30/2019 | Agfa N.V. |
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