FDA 510(k) Applications Submitted by DORNIER MEDTECH AMERICA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170122 | 01/13/2017 | Delta III Lithotripter | Dornier MedTech America |
| K180350 | 02/08/2018 | Dornier Medilas H Solvo 35 Laser | Dornier MedTech America |
| K151298 | 05/15/2015 | Gemini XXP-HP | Dornier MedTech America |
| K132672 | 08/27/2013 | EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER | DORNIER MEDTECH AMERICA |
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