Medical Device Recalls
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1 result found
510(K) Number: K103053 |
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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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VERIFY® SixCess 270FP Challenge Pack, STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, 440-3... | 2 | 03/10/2014 | Steris Corporation |
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