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510k Database
Manufacturers
DK
Medart A/S
Medical Device Manufacturer
·
DK , Hvidovre
Medart A/S - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 2009
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medart A/S
General & Plastic Surgery
✕
3
devices
1-3 of 3
Filters
Cleared
Jun 13, 2012
MEDART 620
K120573
·
GEX
General & Plastic Surgery
·
107d
Cleared
Jun 28, 2011
MEDART DIODE LASER SYSTEM & ACCESSORIES
K110243
·
GEX
General & Plastic Surgery
·
152d
Cleared
Nov 24, 2009
MEDART MODEL 610 CO2 LASER SYSTEM & ACCESSORIES
K083123
·
GEX
General & Plastic Surgery
·
398d
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3
General & Plastic Surgery
3