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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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