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.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Jumper Medical Equipment Co., Ltd.
- Product code
- 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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More clearances from Shenzhen Jumper Medical Equipment Co., Ltd.
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