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..
Clearance details
- Applicant
- Shenzhen Dongdixin Technology Co., Ltd.
- Product code
- Code IPF
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.