FDA 510(k) Applications Submitted by BURK BRANDT

FDA 510(k) Number Submission Date Device Name Applicant
K023218 09/26/2002 MODIFICATION TO PLEXOLONG SETS PAJUNK GMBH
K000722 03/03/2000 UNIPOLAR NEEDLES PAJUNK GMBH
K013041 09/10/2001 PLEXOLONG SETS PAJUNK GMBH
K033018 09/26/2003 STIMULONG PLUS CATHETER SET MODEL, VARIOUS PAJUNK GMBH
K042979 10/29/2004 MODIFICATION TO: PLEXALONG SETS PAJUNK GMBH
K043130 11/12/2004 MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS PAJUNK GMBH


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