FDA 510(k) Applications Submitted by DYNE Medical Group Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240203 | 01/25/2024 | URUS System (DMG-SU100/URUS); URUS System (DMG-SU100R/URUS); URUS System (VP-100/Video Processor) | DYNE Medical Group Inc. |
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