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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K181740
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000 2 07/11/2022 Zeltiq Aesthetics, Inc
CoolCore ZELTIQ Vacuum Applicator REF BRZ-AP1-063-000 2 07/11/2022 Zeltiq Aesthetics, Inc
CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000 2 07/11/2022 Zeltiq Aesthetics, Inc
CoolCurve+ ZELTIQ Vacuum Applicator REF BRZ-AP1-064-000 2 07/11/2022 Zeltiq Aesthetics, Inc
CoolCurve ZELTIQ Vaccum Applicator REF BRZ-AP1-062-000 2 07/11/2022 Zeltiq Aesthetics, Inc
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