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MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233201
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2024
Days to Decision
181 days
Submission Type
Summary

MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233201
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2024
Days to Decision
181 days
Submission Type
Summary