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Penumbra LP Coil System

Page Type
Cleared 510(K)
510(k) Number
K230284
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
265 days
Submission Type
Summary

Penumbra LP Coil System

Page Type
Cleared 510(K)
510(k) Number
K230284
510(k) Type
Traditional
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2023
Days to Decision
265 days
Submission Type
Summary