510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K202470Substantially Equivalent

Li-Battery powered OTC TENS/EMS, model EM-6000, EM-6100, EM-6200 & EM-6300

Everyway Medical Instruments Co., Ltd., Shenkeng District, New Taipei City, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K202470 is the FDA 510(k) clearance record for Li-Battery powered OTC TENS/EMS, model EM-6000, EM-6100, EM-6200 & EM-6300, a class II device, cleared for Everyway Medical Instruments Co.,Ltd on under FDA product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter). FDA's definition for product code NUH reads: "TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES". FDA records list 29 510(k) clearances for Everyway Medical Instruments Co.,Ltd, from to . As of , FDA records show no recalls naming K202470.

Clearance record

Decision date
Received
(89 days to decision)
Product code
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Everyway Medical Instruments Co.,Ltd 3fl., # 5, Ln. 155, Section 3, Peishen Rd.,, Shenkeng District, New Taipei City, CN
510(k) summary
Statement
Third party review
No

Clearances, product code NUH

Trailing 12 months
10 clearances under product code NUH in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NUH, trailing twelve months
MonthClearances
November 20253
December 20253
January 20260
February 20260
March 20261
April 20260
May 20260
June 20262
July 20260
August 20260
September 20261
October 20260