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FDA 510(k) Application Details - K011705
Device Classification Name
Alloy, Metal, Base
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510(K) Number
K011705
Device Name
Alloy, Metal, Base
Applicant
AMERICAN DENT-ALL, INC.
5140 SAN FERNANDO RD.
GLENDALE, CA 91204 US
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Contact
VACHAKAN H KHOIE
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Regulation Number
872.3710
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Classification Product Code
EJH
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More FDA Info for this Product Code
Date Received
06/04/2001
Decision Date
08/03/2001
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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