Everyway Analog OTC TENS— 510(k) K222488
Substantially EquivalentEveryway Medical Instruments Co.,Ltd
FDA 510(k) clearance K222488 for Everyway Analog OTC TENS, Substantially Equivalent on 2022-11-15. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.
Clearance details
- Applicant
- Everyway Medical Instruments 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
- Shenkeng District, New Taipei City, TW
Recent devices under product code NUH
view allMore clearances from Everyway Medical Instruments Co.,Ltd
view all- K251856 — Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4
- K213116 — Everyway Incontinence Stimulation System
- K202849 — Everyway Analog OTC TENS, model N103A/N302
- K202470 — Li-Battery powered OTC TENS/EMS, model EM-6000, EM-6100, EM-6200 & EM-6300
- K202317 — Li-Battery powered OTC TENS/EMS, model EV-804, model EV-805, & model EV-806
Data sourced from openFDA. This site is unofficial and independent of the FDA.