Medical Device Recalls
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1 result found
510(K) Number: K083097 |
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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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Amsco® V-PRO 1 and Amsco® V-PRO 1 Plus Low Temperature Sterilization Systems Model #MLR, Serial # 03... | 2 | 08/19/2011 | Steris Corporation |
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