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FDA 510(k) Applications Submitted by Ethicon Endo-Surgery LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190937
04/10/2019
Echelon Endopath Staple Line Reinforcement
Ethicon Endo-Surgery LLC
K201280
05/13/2020
Ethicon Circular Stapler, Ethicon Circular Stapler -XL Sealed
Ethicon Endo-Surgery LLC
K221343
05/09/2022
ECHELON ENDOPATH Staple Line Reinforcement
Ethicon Endo-Surgery LLC
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