Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K090209 |
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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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| ACL ELITE PRO-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coag... | 2 | 09/30/2024 |
FEI # 1217183 Instrumentation Laboratory |
| ACL ELITE- Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagula... | 2 | 09/30/2024 |
FEI # 1217183 Instrumentation Laboratory |
| ACL ELITE PRO Refurbished)-Analyzer designed specifically for clinical use in the hemostasis laborat... | 2 | 09/30/2024 |
FEI # 1217183 Instrumentation Laboratory |
| ACL ELITE Refurbished-Analyzer designed specifically for clinical use in the hemostasis laboratory, ... | 2 | 09/30/2024 |
FEI # 1217183 Instrumentation Laboratory |
| HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfraction... | 2 | 10/19/2021 |
FEI # 1217183 Instrumentation Laboratory |
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