FDA 510(k) Applications Submitted by ALEXANDER POPP

FDA 510(k) Number Submission Date Device Name Applicant
K050317 02/09/2005 BURANE XL WAVELIGHT LASER TECHNOLOGIE AG
K071183 04/30/2007 ALLEGRO OCULYZER WAVELIGHT AG
K051399 05/31/2005 WAVELIGHT AURIGA WAVELIGHT LASER TECHNOLOGIE AG
K052806 10/04/2005 BURANE WAVELIGHT LASER TECHNOLOGIE AG


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