FDA 510(k) Applications Submitted by JOHN HOFFER

FDA 510(k) Number Submission Date Device Name Applicant
K170122 01/13/2017 Delta III Lithotripter Dornier MedTech America
K910492 02/05/1991 BARD REPLACEMENT GASTROSTOMY TUBE C.R. BARD, INC.
K110364 02/07/2011 DORNIER MEDILAS D LITEBEAM+ 1470 DORNIER MEDTECH AMERICA, INC.
K180350 02/08/2018 Dornier Medilas H Solvo 35 Laser Dornier MedTech America
K130344 02/11/2013 DORNIER MEDILAS UROPULSE DORNIER MEDTECH AMERICA, INC.
K910653 02/14/1991 TOUCHLESS II INTERMITTENT CATHETER C.R. BARD, INC.
K130729 03/18/2013 EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER DORNIER MEDTECH SYSTEMS
K151298 05/15/2015 Gemini XXP-HP Dornier MedTech America
K151485 06/02/2015 GENESIS DORNIER MEDTECH AMERICA, INC.
K121656 06/05/2012 GEMINI LITHOTRIPTER DORNIER MEDTECH AMERICA, INC.
K161771 06/28/2016 Medilas H Laser Fibers DORNIER MEDTECH AMERICA, INC.
K121938 07/02/2012 MEDILAS H RFID LASER FIBER DORNIER MEDTECH AMERICA, INC.
K172084 07/10/2017 Delta III Lithotripter Dornier MedTech America, Inc.
K122159 07/20/2012 DORNIER MEDILAS H30 SOLVO DORNIER MEDTECH AMERICA, INC.
K132672 08/27/2013 EXTRA CORPOREAL SHOCKWAVE LITHOTRIPTER DORNIER MEDTECH AMERICA
K152591 09/10/2015 Medilas H RFID Laser Fibers Dornier MedTech America, Inc.
K935096 10/22/1993 BIOLEX IMPREGNATED WOUND DRESSING C.R. BARD, INC.
K123385 11/02/2012 MEDILAS H LASER FIBERS DORNIER MEDTECH AMERICA, INC.
K133434 11/08/2013 GENESIS II DORNIER MEDTECH AMERICA, INC.


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