FDA 510(k) Applications Submitted by MYTECH TECHNOLOGY CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K030221 01/21/2003 MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR MYTECH TECHNOLOGY CO., LTD.
K041228 05/10/2004 MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 MYTECH TECHNOLOGY CO., LTD.
K061959 07/11/2006 MYTECH / HAPPY LIFE / MAXIAIDS ARM BLOOD PRESSURE MONITOR, HPL-301, HPL-302, HPL-310, 180310 MYTECH TECHNOLOGY CO., LTD.
K030561 02/21/2003 MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODELS HPL-100 AND HPL-100A MYTECH TECHNOLOGY CO., LTD.


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