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FDA 510(k) Application Details - K020833
Device Classification Name
Unit, Operative Dental
More FDA Info for this Device
510(K) Number
K020833
Device Name
Unit, Operative Dental
Applicant
BOYD INDUSTRIES, INC.
12900 44TH ST. NORTH
CLEARWATER, FL 33762 US
Other 510(k) Applications for this Company
Contact
BRUCE LIVINGSTON
Other 510(k) Applications for this Contact
Regulation Number
872.6640
More FDA Info for this Regulation Number
Classification Product Code
EIA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/14/2002
Decision Date
08/08/2002
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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