K233536
- 510(k) number
- K233536
- Device name
- Air Compression Recovery System
- Applicant
- Shenzhen Dongjilian Medical Tech Co., Ltd. CN
- Product code
- IRP — Massager, Powered Inflatable Tube
- Decision date
- 2023-12-16
- Date received
- 2023-11-03
- 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: K233536
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.