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FDA 510(k) Application Details - K024214
Device Classification Name
Alloy, Metal, Base
More FDA Info for this Device
510(K) Number
K024214
Device Name
Alloy, Metal, Base
Applicant
KAVO AMERICA
340 EAST MAIN ST.
LAKE ZURICH, IL 60047 US
Other 510(k) Applications for this Company
Contact
JOHN R FRANZ
Other 510(k) Applications for this Contact
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
12/20/2002
Decision Date
03/12/2003
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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