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Penumbra LP Coil System

Page Type
Cleared 510(K)
510(k) Number
K192955
510(k) Type
Special
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2019
Days to Decision
30 days
Submission Type
Summary

Penumbra LP Coil System

Page Type
Cleared 510(K)
510(k) Number
K192955
510(k) Type
Special
Applicant
Penumbra, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2019
Days to Decision
30 days
Submission Type
Summary