FDA 510(k) Applications Submitted by Dornier MedTech America, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220871 | 03/25/2022 | Nautilus | Dornier MedTech America, Inc |
| K221903 | 06/30/2022 | Delta III Pro | Dornier MedTech America, Inc |
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