FDA 510(k) Applications Submitted by TRULY INSTRUMENT CO., LTD.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K113083 |
10/18/2011 |
TRULY AUTOMATIC ARM BLOOD PRESSURE MONITOR |
TRULY INSTRUMENT CO., LTD. |
K113085 |
10/18/2011 |
TRYLY AUTOMATIC WRIST BLOOD PRESSURE MONITOR |
TRULY INSTRUMENT CO., LTD. |
K091415 |
05/13/2009 |
TRULY AUTOMATIC WRIST BLOOD PRESSURE MONITOR, MODEL DW100,DW200, DW500,DW700,DW703,DW701M.702M |
TRULY INSTRUMENT CO., LTD. |
K091434 |
05/13/2009 |
TRULY AUTOMATIC ARM BLOOD PRESSURE MONITORDB21,DB31,DB22,DB23,DB71M,DB32,DB61M, DB62M, DB63M |
TRULY INSTRUMENT CO., LTD. |
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