Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K800826 |
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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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Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --... | 2 | 07/25/2017 | Fisher Diagnostics |
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 10... | 2 | 07/25/2017 | Fisher Diagnostics |
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