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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