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FDA 510(k) Application Details - K962785
Device Classification Name
Agent, Tooth Bonding, Resin
More FDA Info for this Device
510(K) Number
K962785
Device Name
Agent, Tooth Bonding, Resin
Applicant
3M COMPANY
3M CENTER
BLDG. 275-3SE-08
ST. PAUL, MN 55144-1000 US
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Contact
SCOTT ERICKSON
Other 510(k) Applications for this Contact
Regulation Number
872.3200
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Classification Product Code
KLE
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More FDA Info for this Product Code
Date Received
07/17/1996
Decision Date
08/12/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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