Wireless Pain Relieve Device Model: LT5018C— 510(k) K173462
Substantially EquivalentShenzhen Dongdixin Technology Co., Ltd.
FDA 510(k) clearance K173462 for Wireless Pain Relieve Device Model: LT5018C, Substantially Equivalent on 2017-12-08. Applicant: Shenzhen Dongdixin Technology Co., Ltd..
Clearance details
- Applicant
- Shenzhen Dongdixin Technology Co., Ltd.
- Product code
- Code NUH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.