FDA 510(k) Applications Submitted by COMMWELL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K103791 12/27/2010 PHYSIOGLOVE ES WITH ECG ANALYSIS COMMWELL LTD.
K083677 12/11/2008 PHYSIOGLOVE FOR USE WITH PHYSIOGLOVE ES1 COMMWELL LTD.
K050674 03/15/2005 PHYSIOGLOVE ES COMMWELL LTD.


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