FDA 510(k) Applications Submitted by Antje Katzer

FDA 510(k) Number Submission Date Device Name Applicant
K150140 01/22/2015 MCL 31 Dermablate ASCLEPION LASER TECHNOLOGIES GMBH
K161257 05/04/2016 MultiPulse HoPLUS ASCLEPION LASER TECHNOLOGIES GMBH
K071451 05/24/2007 TATTOOSTAR Y ASCLEPION LASER TECHNOLOGIES GMBH
K081541 06/02/2008 DERMABLATE EFFECT ASCLEPION LASER TECHNOLOGIES GMBH
K131757 06/17/2013 TATTOOSTAR EFFECT COMBO ASCLEPION LASER TECHNOLOGIES GMBH
K131987 06/28/2013 MULTIPULSE HOPLUS ASCLEPION LASER TECHNOLOGIES GMBH
K111851 06/29/2011 MEDIOSTAR NEXT ASCLEPION LASER TECHNOLOGIES GMBH
K152153 08/03/2015 MicroSpot Handpiece ASCLEPION LASER TECHNOLOGIES GMBH
K192483 09/10/2019 MeDioStar ASCLEPION LASER TECHNOLOGIES GMBH
K112669 09/14/2011 TATTOOSTAR EFFECT Y ASCLEPION LASER TECHNOLOGIES GMBH
K133297 10/25/2013 QUADROSTARPROGREEN, QUADROSTARPROYELLOW ASCLEPION LASER TECHNOLOGIES GMBH
K113489 11/23/2011 ORION ASCLEPION LASER TECHNOLOGIES GMBH
K143519 12/12/2014 The MeDioStar NeXT Family ASCLEPION LASER TECHNOLOGIES GMBH
K133891 12/20/2013 MULTIPULSE TM+1470 ASCLEPION LASER TECHNOLOGIES GMBH


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