Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K050673 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-00-0320 Vbeam Aesthetica w/ ... | 2 | 02/15/2007 |
FEI # 1218402 Candela Laser Corporation |
| Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gynecology, ... | 2 | 05/04/2006 |
FEI # 1218402 Candela Laser Corporation |
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