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FDA 510(k) Application Details - K970129
Device Classification Name
Material, Impression
More FDA Info for this Device
510(K) Number
K970129
Device Name
Material, Impression
Applicant
RICHARD TING
1510 SOUTH BROAD ST.
PHILADELPHIA, PA 19146 US
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Contact
RICHARD TING
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Regulation Number
872.3660
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Classification Product Code
ELW
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More FDA Info for this Product Code
Date Received
01/15/1997
Decision Date
08/18/1997
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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