K233804
- 510(k) number
- K233804
- Device name
- Resonic Rapid Acoustic Pulse Device
- Applicant
- Zeltiq Aesthetics, Inc. CA · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-02-01
- Date received
- 2023-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K233804.pdf
Official FDA record: K233804
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.