Medical Device Recalls
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1 result found
510(K) Number: K081360 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PATHFAST Myoglobin II reagent cartridge Catalog Number: PF1111-K PATHFAST® NTproBNP is a product... | 2 | 09/17/2018 |
FEI # 1000119795 Polymedco, Inc.,/Polymedco Cancer Diagnostic Products, Llc |
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