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FDA 510(k) Applications Submitted by SHELLY HENRY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060153
01/20/2006
ACUMED LASER, MODEL 1000
LASER THERA, LLC
K082223
08/06/2008
NEUTROLUMENPN SYSTEM, MODEL 1000
NEUROLUMEN, LLC
K063745
12/19/2006
MEDILASER, MODEL 1000
LASER THERA, LLC
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