FDA 510(k) Applications Submitted by ROSSMAX INTERNATIONL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K010190 01/22/2001 WRISTWATCH BLOOD PRESSURE MONITOR, MODEL A43 ROSSMAX INTERNATIONL LTD.
K010498 02/21/2001 WRISTWATCH BLOOD PRESSURE MONITOR A46 ROSSMAX INTERNATIONL LTD.
K020897 03/19/2002 ROSSMAX AUTOMATIC WRIST BLOOD PRESSURE MONITOR, MODELS B150 & Q400 ROSSMAX INTERNATIONL LTD.
K053006 10/26/2005 ROSSMAX DIGITAL SPHYGMOMANOMETER MANDAUS II ROSSMAX INTERNATIONL LTD.


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