K251623
- 510(k) number
- K251623
- Device name
- Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)
- Applicant
- Shenzhen Yicai Health Technology Co., Ltd. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2025-09-17
- Date received
- 2025-05-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K251623
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.