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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K111822
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STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid Anti-Xa kits are intended f... 2 08/28/2025 FEI # 2245451
Diagnostica Stago, Inc.
STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended ... 2 08/28/2025 FEI # 2245451
Diagnostica Stago, Inc.
Stago IVD, Liquid Anti-Xa, NDC 3607450003116. The STA - Liquid Anti-Xa kits are intended for use ... 3 09/16/2014 FEI # 2245451
Diagnostica Stago, Inc.
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