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PORTACLAMP FLEX

Page Type
Cleared 510(K)
510(k) Number
K070380
510(k) Type
Traditional
Applicant
CARDIO LIFE RESEARCH, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2007
Days to Decision
120 days
Submission Type
Summary

PORTACLAMP FLEX

Page Type
Cleared 510(K)
510(k) Number
K070380
510(k) Type
Traditional
Applicant
CARDIO LIFE RESEARCH, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2007
Days to Decision
120 days
Submission Type
Summary