Mini TENS Therapy Device— 510(k) K182871
Substantially EquivalentShenzhen Jumper Medical Equipment Co., Ltd.
FDA 510(k) clearance K182871 for Mini TENS Therapy Device, Substantially Equivalent on 2019-08-01. Applicant: Shenzhen Jumper Medical Equipment Co., Ltd..
Clearance details
- Applicant
- Shenzhen Jumper Medical Equipment Co., Ltd.
- Product code
- Code NUH
- Advisory panel
- Neurology
- 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.