FDA 510(k) Applications Submitted by STEVE G HUTSON

FDA 510(k) Number Submission Date Device Name Applicant
K050216 01/31/2005 OMNILUX REVIVE AND OMNILUX PLUS PHOTO THERAPEUTICS LIMITED
K043329 12/02/2004 OMNILUX REVIVE AND BLUE PHOTO THERAPEUTICS LIMITED
K043317 12/02/2004 OMNILUX PLUS PHOTO THERAPEUTICS LIMITED


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