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Lantern Delivery Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K152840
510(k) Type
Special
Applicant
PENUMBRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2015
Days to Decision
64 days
Submission Type
Summary

Lantern Delivery Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K152840
510(k) Type
Special
Applicant
PENUMBRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2015
Days to Decision
64 days
Submission Type
Summary