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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K171069

ZELTIQ CoolSculpting System · Zeltiq Aesthetics, Inc. · decided 2017-07-07 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Sealed CoolMini ApplicatorCS-300650 Zeltiq Aesthetics, Inc.OOK00816417021190
CoolMicro ApplicatorCS-300684Zeltiq Aesthetics, Inc.OOK00816417021206