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U.S. Department of Health and Human Services

Medical Device Recalls
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Recall Date to: 08/02/2015 510(K) Number: K050673
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Product Description
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FDA Recall
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Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-00-0320 Vbeam Aesthetica w/ ... 2 02/15/2007 Candela Laser Corporation
Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gynecology, ... 2 05/04/2006 Candela Laser Corporation
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