Medical Device Recalls
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1 result found
510(K) Number: K092669 |
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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 DX-D Imaging Package - (The detector power cables described in the Report of Correction and Rem... | 2 | 02/19/2012 | AGFA Corp. |
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