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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