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Copd Partners, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K072011
COPD LIQUID OXYGEN PORTABLE, MODEL 300P
October 18, 2007
K071461
MODEL 300D HOME OXYGEN LIQUEFIER
August 21, 2007