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MIVI 6F GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K140557
510(k) Type
Traditional
Applicant
MIVI, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2014
Days to Decision
197 days
Submission Type
Summary

MIVI 6F GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K140557
510(k) Type
Traditional
Applicant
MIVI, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2014
Days to Decision
197 days
Submission Type
Summary