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FDA 510(k) Applications Submitted by MIKI KOLTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070690
03/13/2007
THE LIFE VESSEL
COTTONWOOD VESSEL CORPORATION
K082969
10/06/2008
LUMINEX INFRARED LAMP SYSTEM
MEDICAL LASER SYSTEMS INC
K063574
11/29/2006
LUMINEX LL LASER SYSTEM
MEDICAL LASER SYSTEMS INC
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