Medical Device Recalls
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1 result found
510(K) Number: K193566 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1... | 2 | 08/27/2021 |
FEI # 3007215625 Zeltiq Aesthetics, Inc |
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