TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)— 510(k) K213788
Substantially EquivalentDongguan Bohuikang Technology Co.,Ltd
FDA 510(k) clearance K213788 for TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080), Substantially Equivalent on 2022-05-06. Applicant: Dongguan Bohuikang Technology Co.,Ltd. Device class: 2.
Clearance details
- Applicant
- Dongguan Bohuikang Technology 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
- Dongguan, CN
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Data sourced from openFDA. This site is unofficial and independent of the FDA.