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MIVI Q Distal Access Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212402
510(k) Type
Special
Applicant
MIVI Neuroscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
136 days
Submission Type
Summary

MIVI Q Distal Access Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212402
510(k) Type
Special
Applicant
MIVI Neuroscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
136 days
Submission Type
Summary