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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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