FDA 510(k) Applications Submitted by Zeltiq Aesthetics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K181740 07/02/2018 ZELTIQ CoolSculpting System ZELTIQ Aesthetics, Inc.
K183514 12/18/2018 ZELTIQ CoolSculpting System ZELTIQ Aesthetics, Inc.
K120023 01/03/2012 ZELTIQ COOLSCULPTING ZELTIQ AESTHETICS, INC.
K222629 08/31/2022 Resonic Rapid Acoustic Pulse Device Zeltiq Aesthetics, Inc.
K160259 02/01/2016 ZELTIQ CoolSculpting System ZELTIQ AESTHETICS, INC.
K171069 04/10/2017 ZELTIQ CoolSculpting System ZELTIQ Aesthetics, Inc.
K151179 05/04/2015 ZELTIQ CoolSculpting System ZELTIQ AESTHETICS, INC.
K142491 09/04/2014 ZEL TIQ CoolSculpting System ZELTIQ AESTHETICS, INC.
K133212 10/18/2013 ZELTIQ COOLSCULPTING SYSTEM ZELTIQ AESTHETICS, INC.
K193566 12/23/2019 ZELTIQ CoolSculpting System ZELTIQ Aesthetics, Inc.
K212707 08/26/2021 CoolSculpting Elite System Zeltiq Aesthetics, Inc.


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