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Everlife Interferential Current Therapy, Model IF-100507

by Everlife Medical Equipment Co., Ltd. 510(k)

Active United States

510(k) K070890

Overview

The Everlife Interferential Current Therapy, Model IF-100507 is a device that delivers interferential current therapy for medical purposes. It is classified as an Interferential Current Therapy device under product code LIH and is intended for use in neurology applications.

The device is manufactured by Everlife Medical Equipment Co., Ltd. and received FDA 510(k) clearance with K number K070890 on June 29, 2007, as substantially equivalent to predicate devices. It is regulated under 882.5890 and is a class II medical device. The device is supplied with various registration numbers and is intended for use in clinical settings under appropriate medical supervision.

AI-generated from registry data, 26 Sep 2026.Not verified by deviCERTS or the manufacturer

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK070890 Date29 Jun 2007ClearedStatusActive

Coverage

1 jurisdiction

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
LIH
Device Class
Class II
Regulation
21 CFR Part 882.5890
Advisory Committee
Neurology
FDA Decision
SESE Substantially Equivalent

Other devices from Everlife Medical Equipment Co., Ltd.

Questions

  • What is the Everlife Interferential Current Therapy Model IF-100507 used for?

    The Everlife Interferential Current Therapy Model IF-100507 is a device that delivers interferential current therapy for medical purposes, specifically intended for use in neurology applications in clinical settings under appropriate medical supervision.

  • What is the regulatory status of the Everlife Interferential Current Therapy Model IF-100507?

    The device received FDA 510(k) clearance with K number K070890 on June 29, 2007, as substantially equivalent to predicate devices. It is regulated under 882.5890 and is classified as a class II medical device.

  • Is the Everlife Interferential Current Therapy Model IF-100507 reusable or single-use?

    The device data does not specify whether the Everlife Interferential Current Therapy Model IF-100507 is designed for single-use or multiple uses. This information would be detailed in the device's instructions for use provided by the manufacturer.

  • What are the specifications of the Everlife Interferential Current Therapy Model IF-100507?

    The Everlife Interferential Current Therapy Model IF-100507 is classified under product code LIH and is manufactured by Everlife Medical Equipment Co., Ltd. It is intended for neurology applications and is supplied with various registration numbers as listed in the device data.