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Indigo Aspiration System - Aspiration Catheter 7 and Separator 7

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193595
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2020
Days to Decision
240 days
Submission Type
Summary

Indigo Aspiration System - Aspiration Catheter 7 and Separator 7

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193595
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2020
Days to Decision
240 days
Submission Type
Summary