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
K233380 10/02/2023 TRIDENT Mobile Fluoroscopy System Dornier MedTech America
K243820 12/12/2024 Hoover Negative Pressure Access Sheath (Hoover) (Hoover Model #'s IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-1250 Dornier MedTech America


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