Medical Device Recalls
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1 result found
510(K) Number: K122236 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The VariSource iX series afterloader systems are computer controlled remote electro/mechanical syste... | 2 | 06/26/2015 |
FEI # 3011400544 Varian Medical Systems Inc |
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