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FDA 510(k) Application Details - K060287
Device Classification Name
Controller, Foot, Handpiece And Cord
More FDA Info for this Device
510(K) Number
K060287
Device Name
Controller, Foot, Handpiece And Cord
Applicant
W & H DENTALWERK BUERMOOS GMBH
IGNAZ GLASER STR. 53
BUERMOOS A-5111 AT
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Contact
GABRIELE WIENBECK
Other 510(k) Applications for this Contact
Regulation Number
872.4200
More FDA Info for this Regulation Number
Classification Product Code
EBW
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More FDA Info for this Product Code
Date Received
02/06/2006
Decision Date
05/03/2006
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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