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FDA 510(k) Application Details - K022184
Device Classification Name
Activator, Ultraviolet, For Polymerization
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510(K) Number
K022184
Device Name
Activator, Ultraviolet, For Polymerization
Applicant
DISCUS DENTAL, INC.
8550 HIGUERA ST.
CULVER CITY, CA 90232-2522 US
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Contact
GARRY L HOLLAR
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Regulation Number
872.6070
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Classification Product Code
EBZ
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More FDA Info for this Product Code
Date Received
07/03/2002
Decision Date
08/20/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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