Medical Device Recalls
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1 result found
510(K) Number: K024260 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Candela Laser GentleLase Pro, Powered Laser Surgical Instrument for dermatological use - Model numbe... | 2 | 11/18/2013 | Candela Corporation |
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