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MIVI Mi-AXUS Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151396
510(k) Type
Traditional
Applicant
MIVI NEUROSCIENCE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2015
Days to Decision
197 days
Submission Type
Summary

MIVI Mi-AXUS Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151396
510(k) Type
Traditional
Applicant
MIVI NEUROSCIENCE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2015
Days to Decision
197 days
Submission Type
Summary