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Cardio Life Research, S.A.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K070380
PORTACLAMP FLEX
June 8, 2007
K033085
PORTACLAMP
April 27, 2004