Biofeedback Nerve and Muscle Stimulator— 510(k) K220161
Substantially EquivalentShenzhen Konmed Technology Co., Ltd.
FDA 510(k) clearance K220161 for Biofeedback Nerve and Muscle Stimulator, Substantially Equivalent on 2022-07-20. Applicant: Shenzhen Konmed Technology Co., Ltd..
Clearance details
- Applicant
- Shenzhen Konmed Technology Co., Ltd.
- Product code
- Code KPI
- Advisory panel
- Gastroenterology, Urology
- 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.