K253076
- 510(k) number
- K253076
- Device name
- Cryopush Cold Compression Device (A02-P-001)
- Applicant
- Chengdu Cryo-Push Medical Technology Co.,Ltd CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2026-04-02
- Date received
- 2025-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K253076.pdf
Official FDA record: K253076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.