Medical Device Recalls
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1 result found
510(K) Number: K103338 |
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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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VariaBreeze; Catalog number: 7300-0035-2. Podiatry: ablation, vaporization, incision, excision... | 2 | 09/30/2016 | New Star Lasers, Inc. |
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