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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name interferential current therapy
510(k) Number K070890
Device Name EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507
Applicant
EVERLIFE MEDICAL EQUIPMENT CO., LTD.
NO. 58, FU-CHIUN STREET
HSIN CHU CITY,  TW 30067
Applicant Contact Ke-Min Jen
Correspondent
EVERLIFE MEDICAL EQUIPMENT CO., LTD.
NO. 58, FU-CHIUN STREET
HSIN CHU CITY,  TW 30067
Correspondent Contact Ke-Min Jen
Regulation Number882.5890
Classification Product Code
LIH  
Date Received03/30/2007
Decision Date 06/29/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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