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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K010853
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Product Description
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Guider Softip XF; GUIDER/ST XF/6FR/100 cm, Model number:M003101500 . Cardiology: Boston Scient... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER MPXF 5F 90CM, Model number: M003100630. Cardiology: Boston Scientific... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER STRAIGHT XF 5F 90CM, Model number: . M003100640. Cardiology: Boston Sc... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER STRAIGHT XF 5F 100CM, Model number: M003101640. Cardiology: Boston Scie... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER/MP XF/8FR/100 cm, Model number: M003101480. Cardiology: Boston Scient... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER/40DEG XF/7FR/90CM, Model number: H965100430 . Cardiology: Boston Scie... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
Guider Softip XF; GUIDER MPXF 5F 100CM, Model number: M003101630. Cardiology: Boston Scientifi... 2 11/02/2016 FEI # 3008853977
Stryker Neurovascular
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