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FDA 510(k) Application Details - K022165
Device Classification Name
Light, Ultraviolet, Dermatological
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510(K) Number
K022165
Device Name
Light, Ultraviolet, Dermatological
Applicant
THERALIGHT, INC.
2794 LOKER AVE. WEST,SUITE 105
CARLSBAD, CA 92008-6616 US
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Contact
RAYMOND HARTMAN
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Regulation Number
878.4630
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Classification Product Code
FTC
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More FDA Info for this Product Code
Date Received
07/03/2002
Decision Date
07/18/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
Y
Expedited Review
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