FDA 510(k) Applications Submitted by Koya Medical, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210885 | 03/25/2021 | Dayspring | Koya Medical, Inc. |
| K212287 | 07/21/2021 | Dayspring Lite | Koya Medical, Inc. |
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