510(k) K233732

Device
CoolSculpting Elite System
Applicant
Zeltiq Aesthetics, Inc. (Acquired by Allergan Aesthetics
510(k) number
K233732
Product code
OOK
Decision
Substantially Equivalent (SESE)
Decision date
2024-09-12
Date received
2023-11-21
Regulation
878.4340
Classification name
Dermal Cooling Pack/Vacuum/Massager
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Victoria Montemayor
Address
And Now, An Abbvie, Inc. Company) 4410 Rosewood Dr. Pleasanton CA US 94588 94588

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00816417023538CoolSculpting EliteZeltiq Aesthetics, Inc.2026-05-22
00816417023088CoolSculpting EliteZeltiq Aesthetics, Inc.2026-05-22
00816417022579CoolSculpting EliteZeltiq Aesthetics, Inc.2026-05-22
00816417022555CoolSculpting EliteZeltiq Aesthetics, Inc.2026-05-22

Other 510(k) Records For Product Code OOK

510(k)DeviceApplicantDecision date
K212707CoolSculpting Elite SystemZeltiq Aesthetics, Inc.2021-11-05
K193566ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2020-01-21
K183514ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2019-01-14
K181740ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2018-08-29
K172144CoolSculpting SystemZeltiq Aesthetics2017-11-01
K171069ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2017-07-07
K162050ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2016-11-21
K160259ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2016-03-23
K151179ZELTIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2015-09-22
K142491ZEL TIQ CoolSculpting SystemZeltiq Aesthetics, Inc.2015-01-26
K133212ZELTIQ COOLSCULPTING SYSTEMZeltiq Aesthetics, Inc.2014-04-09
K120023ZELTIQ COOLSCULPTINGZeltiq Aesthetics, Inc.2012-05-02
DEN090002ZELTIQ AESTHETICS DERMAL COOLING DEVICEZeltiq Aesthetics2010-08-24