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FDA 510(k) Application Details - K083179
Device Classification Name
Unit, Neonatal Phototherapy
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510(K) Number
K083179
Device Name
Unit, Neonatal Phototherapy
Applicant
MEDIX I.C.S.A.
11874 SOUTH EVELYN CIRCLE
HOUSTON, TX 77071 US
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Contact
J. HARVEY KNAUSS
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Regulation Number
880.5700
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Classification Product Code
LBI
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More FDA Info for this Product Code
Date Received
10/28/2008
Decision Date
02/27/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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