K230524
- 510(k) number
- K230524
- Device name
- Cold Compression Wrap Pro
- Applicant
- Chengdu Cryo-Push Medical Technology Co.,Ltd CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2024-01-19
- Date received
- 2023-02-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K230524.pdf
Official FDA record: K230524
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.