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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
K222948
510(k) Type
Traditional
Applicant
MIVI Neuroscience, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2023
Days to Decision
357 days
Submission Type
Summary

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
K222948
510(k) Type
Traditional
Applicant
MIVI Neuroscience, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2023
Days to Decision
357 days
Submission Type
Summary