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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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