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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 46 of 46 Results
510(K) Number: K041585
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Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, sterile, REF 0535-60... 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, sterile, ... 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute... 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute... 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute... 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Stryker 100 mL AutoFuser PainPump, single site continuous, 2.0 mL/hr, sterile, REF 0531-200-000. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
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