Last synced on 14 November 2025 at 11:06 pm

MIVI Mi-AXUS Guide Catheter

Page Type
Cleared 510(K)
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)
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