FDA 510(k)

EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507

K-Number: K070890 · 2007-06-29

ApplicantEverlife Medical Equipment Co., Ltd.

Decision Date2007-06-29

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 is the device name listed in this FDA 510(k) record. The listed applicant is Everlife Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2007-06-29 under 510(k) number K070890. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507?

EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 is a medical device that received FDA 510(k) clearance on 2007-06-29. The listed applicant is Everlife Medical Equipment Co., Ltd.. The 510(k) number is K070890.

When did EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 receive FDA 510(k) clearance?

EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 received FDA 510(k) clearance on 2007-06-29, under 510(k) number K070890.

Who is the listed applicant for EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507?

The FDA 510(k) record lists Everlife Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507?

The FDA product code for EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 is LIH.

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Other records listing Everlife Medical Equipment Co., Ltd. as applicant

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Related Devices (Code: LIH)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.