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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