Combo Stimulator MT9000, Combo Stimulator LT7102, TENS Stimulator InTENSity 10— 510(k) K171978
Substantially EquivalentShenzhen Dongdixin Technology Co., Ltd.
FDA 510(k) clearance K171978 for Combo Stimulator MT9000, Combo Stimulator LT7102, TENS Stimulator InTENSity 10, Substantially Equivalent on 2017-10-02. Applicant: Shenzhen Dongdixin Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Dongdixin Technology Co., Ltd.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code IPF
view allMore clearances from Shenzhen Dongdixin Technology Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.