FDA 510(k) Applications Submitted by Dornier MedTech America Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190612 | 03/11/2019 | EQUINOX Balloon Dilatation Catheter | Dornier MedTech America Inc |
| K191187 | 05/03/2019 | Dornier MINNOW Ureteral Catheter | Dornier MedTech America Inc |
| K201815 | 07/01/2020 | Dornier MAGELLAN Ureteral Access Sheath | Dornier MedTech America Inc |
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