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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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