Medical Device Recalls
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1 result found
510(K) Number: K172319 |
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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, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems The V-PRO 1, V-... | 2 | 08/31/2018 | Steris Corporation |
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