Everyway Wireless TENS & EMS Unit
K-Number: K181707 · 2018-09-26
Device Summary
Frequently Asked Questions
What is the Everyway Wireless TENS & EMS Unit?
Everyway Wireless TENS & EMS Unit is a medical device that received FDA 510(k) clearance on 2018-09-26. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K181707.
When did Everyway Wireless TENS & EMS Unit receive FDA 510(k) clearance?
Everyway Wireless TENS & EMS Unit received FDA 510(k) clearance on 2018-09-26, under 510(k) number K181707.
Who is the listed applicant for Everyway Wireless TENS & EMS Unit?
The FDA 510(k) record lists Everyway Medical Instruments Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Everyway Wireless TENS & EMS Unit?
The FDA product code for Everyway Wireless TENS & EMS Unit is NUH.
Other records listing Everyway Medical Instruments Co.,Ltd as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NUH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.