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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K152570
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Product Description
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FDA Recall
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J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used f... 2 10/19/2018 Bovie Medical Corporation
BVX-330NR Bovie Precise 360 Handpiece 33cm, needle Product is used for the delivery of helium g... 2 08/25/2016 Bovie Medical Corporation
BVX-450NR Bovie Precise 360 Handpiece 45cm, needle Product is used for the delivery of helium g... 2 08/25/2016 Bovie Medical Corporation
BVX-330BR Bovie Precise 360 Handpiece 33cm, blade Product is used for the delivery of helium ga... 2 08/25/2016 Bovie Medical Corporation
BVX-450BR Bovie Precise 360 Handpiece 45cm, blade Product is used for the delivery of helium gas ... 2 08/25/2016 Bovie Medical Corporation
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