FDA 510(k) Applications Submitted by ViewRay, Incorporated
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181989 | 07/26/2018 | MRIdian Linac System | ViewRay, Incorporated |
| K212958 | 09/16/2021 | MRIdian Linac System | ViewRay, Incorporated |
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