FDA 510(k) Applications Submitted by Adam Viitala
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180151 | 01/19/2018 | MC3 Jugular Dual Lumen Catheter | MC3 Incorporated |
| K191935 | 07/19/2019 | Nautilus Smart ECMO Module | MC3 Incorporated |
| K182914 | 10/18/2018 | MC3 Vascular Access Kit 21030 | MC3 Incorporated |
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