Medical Device Recalls
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1 result found
510(K) Number: K052947 |
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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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M-19 (Iridium 192): Source Production and Equipment Company, St. Rose, LA. Brachytherapy source. | 2 | 06/25/2015 | Source Production & Equipment Inc |
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