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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: K861985
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GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastom... 2 04/08/2020 FEI # 1417572
Baxter Healthcare Corporation
GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended to be used in the anastomo... 2 04/08/2020 FEI # 1417572
Baxter Healthcare Corporation
GEM Microvascular Anastomotic Coupler Devices s intended to be used in the anastomosis of veins and ... 2 04/08/2020 FEI # 1417572
Baxter Healthcare Corporation
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