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FDA 510(k) Application Details - K060080
Device Classification Name
Caries Detector, Laser Light, Transmission
More FDA Info for this Device
510(K) Number
K060080
Device Name
Caries Detector, Laser Light, Transmission
Applicant
KAVO DENTAL CORPORATION
PO BOX 7007
DEERFIELD, IL 60015 US
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Contact
DANIEL KAMM
Other 510(k) Applications for this Contact
Regulation Number
872.1745
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Classification Product Code
NTK
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More FDA Info for this Product Code
Date Received
01/10/2006
Decision Date
02/08/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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