Zeltiq Aesthetics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Zeltiq Aesthetics, Inc.
Recent clearances by Zeltiq Aesthetics, Inc.
- K233804 — Resonic Rapid Acoustic Pulse Device
- K222629 — Resonic Rapid Acoustic Pulse Device
- K212707 — CoolSculpting Elite System
- K193566 — ZELTIQ CoolSculpting System
- K183514 — ZELTIQ CoolSculpting System
- K181740 — ZELTIQ CoolSculpting System
- K171069 — ZELTIQ CoolSculpting System
- K162050 — ZELTIQ CoolSculpting System
- K160259 — ZELTIQ CoolSculpting System
- K151179 — ZELTIQ CoolSculpting System
- K142491 — ZEL TIQ CoolSculpting System
- K133212 — ZELTIQ COOLSCULPTING SYSTEM
- K120023 — ZELTIQ COOLSCULPTING
Data sourced from openFDA. This site is unofficial and independent of the FDA.