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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