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FDA 510(k) Application Details - K123929
Device Classification Name
Alloy, Metal, Base
More FDA Info for this Device
510(K) Number
K123929
Device Name
Alloy, Metal, Base
Applicant
BEGO BREMER GOLDSCHLAEGEREI WILH. HERBST GMBH & CO
WILHELM-HERBST-STRASSE 1
BREMEN 28359 DE
Other 510(k) Applications for this Company
Contact
HEIKE GUSTKE
Other 510(k) Applications for this Contact
Regulation Number
872.3710
More FDA Info for this Regulation Number
Classification Product Code
EJH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/20/2012
Decision Date
03/14/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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