Air Compression Therapy System— 510(k) K192466
Substantially EquivalentShenzhen Lifotronic Technology Co., Ltd.
FDA 510(k) clearance K192466 for Air Compression Therapy System, Substantially Equivalent on 2020-06-22. Applicant: Shenzhen Lifotronic Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Lifotronic Technology Co., Ltd.
- Product code
- Code IRP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5650
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code IRP
view allMore clearances from Shenzhen Lifotronic Technology Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.