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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Date Classified to: 10/25/2014 510(K) Number: K050673
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Product Description
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Recall
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Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-00-0320 Vbeam Aesthetica w/ ... 2 Feb-15-2007 Candela Laser Corporation
Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-08-0320 Vbeam Aesthetica w/ ... 2 Feb-15-2007 Candela Laser Corporation
Candela Corporation Vbeam Perfecta Laser System, Model/Catalog # 9914-08-0300 Vbeam Perfecta w/ gray... 2 Feb-15-2007 Candela Laser Corporation
Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-08-0310 Vbeam Platinum w/ gray... 2 Feb-15-2007 Candela Laser Corporation
Candela Corporation Vbeam Perfecta Laser System, Model/Catalog # 9914-00-0300 Vbeam Perfecta w/ rose... 2 Feb-15-2007 Candela Laser Corporation
Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-00-0310 Vbeam Platinum w/ rose... 2 Feb-15-2007 Candela Laser Corporation
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