FDA 510(k) Applications Submitted by Fujio Zushi
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190509 | 03/01/2019 | Lubrina 2 | J. Morita USA, Inc. |
| K201378 | 05/26/2020 | 3D Accuitomo 150N | J. Morita USA, INC. |
| K213477 | 10/29/2021 | Root ZX3 | J. Morita USA, Inc. |
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