← Back to catalogue
ShockPhysio Mobile (model SW3200 Basic)
FDA 510(k)Class I (US FDA 510(k))
510(k) K240358
Identifiers
- 510(k) Number
- K240358 FDA 510(k)
- FDA Product Code
- ISA FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 890.5660 FDA 510(k)
- Regulation Number
- 890.5660 FDA 510(k)
- Advisory Committee
- Physical Medicine FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
ShockPhysio Mobile (model SW3200 Basic) by Shenzhen Dongdixin Technology Co., Ltd. — Class I — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K240358 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shenzhen Dongdixin Technology Co., Ltd.
Sources (1)
- FDA 510(k) K240358 24 fields · synced Jun 18, 2026