Medical Device Recalls
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1 result found
510(K) Number: K060200 |
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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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| Maximal Barrier Drape; Product Codes: ASK-00002-1A | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
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