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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