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PORTACLAMP FLEX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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