FDA 510(k) Applications Submitted by Viseon, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191579 | 06/14/2019 | Voyant System | Viseon, Inc. |
| K181885 | 07/13/2018 | Voyant System | Viseon, Inc. |
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