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Commwell , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103791PHYSIOGLOVE ES WITH ECG ANALYSISOctober 21, 2011
K083677PHYSIOGLOVE FOR USE WITH PHYSIOGLOVE ES1March 10, 2009
K050674PHYSIOGLOVE ESApril 25, 2006