Smart Pain Reliever, Model LT5019— 510(k) K162479
Substantially EquivalentShenzhen Dongdixin Technology Co., Ltd.
FDA 510(k) clearance K162479 for Smart Pain Reliever, Model LT5019, Substantially Equivalent on 2017-02-08. Applicant: Shenzhen Dongdixin Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Dongdixin Technology Co., Ltd.
- Product code
- Product code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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