Medical Device Recalls
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1 result found
510(K) Number: K897045 |
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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® Bowie-Dick Test Card, Model #S3098, Steris Biological Operations, 9325 Pinecone Drive, Mento... | 2 | 09/20/2012 | Steris Corporation |
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