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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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