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FDA 510(k) Applications Submitted by TUNG FU ELECTRIC CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042107
08/04/2004
TUNG FU AIRMATE TENS, VITALITY MODE, TF-DT001
TUNG FU ELECTRIC CO., LTD.
K061452
05/25/2006
TF-BP01 BLOOD PRESSURE MEASUREMENT SYSTEM
TUNG FU ELECTRIC CO., LTD.
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