Air Compression Therapy Device, model: ST-502— 510(k) K213745
Substantially EquivalentShenzhen Future Electronic Co., Ltd.
FDA 510(k) clearance K213745 for Air Compression Therapy Device, model: ST-502, Substantially Equivalent on 2022-03-31. Applicant: Shenzhen Future Electronic Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Future Electronic 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
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