Transcutaneous Electrical Nerve Stimulator, Model: KTR-405— 510(k) K220998
Substantially EquivalentShenzhen Kentro Medical Electronics Co., Ltd.
FDA 510(k) clearance K220998 for Transcutaneous Electrical Nerve Stimulator, Model: KTR-405, Substantially Equivalent on 2022-08-24. Applicant: Shenzhen Kentro Medical Electronics Co., Ltd..
Clearance details
- Applicant
- Shenzhen Kentro Medical Electronics 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.