Air Compression Massager (Model LF-FT003)— 510(k) K213000
Substantially EquivalentWenzhou Lingfeng Electronic Technology Co., Ltd.
FDA 510(k) clearance K213000 for Air Compression Massager (Model LF-FT003), Substantially Equivalent on 2021-11-15. Applicant: Wenzhou Lingfeng Electronic Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Wenzhou Lingfeng Electronic 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
- Ruian, CN
Recent devices under product code IRP
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