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FDA 510(k) Application Details - K960833
Device Classification Name
Purifier, Air, Ultraviolet, Medical
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510(K) Number
K960833
Device Name
Purifier, Air, Ultraviolet, Medical
Applicant
UV TECHNOLOGIES, INC.
1129 BLOOMFIELD AVE.
WEST CALDWELL, NJ 07006 US
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Contact
ANNE MARIE CESARIO
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Regulation Number
880.6500
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Classification Product Code
FRA
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More FDA Info for this Product Code
Date Received
02/29/1996
Decision Date
07/25/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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