Medical Device Recalls
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1 result found
510(K) Number: K082721 |
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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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The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber... | 2 | 10/01/2013 | PhotoMedex, Inc. |
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