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FDA 510(k) Application Details - K021298
Device Classification Name
Tester, Pulp
More FDA Info for this Device
510(K) Number
K021298
Device Name
Tester, Pulp
Applicant
SYBRON ENDO/ANALYTIC
1717 WEST COLLINS AVE.
ORANGE, CA 92867 US
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Contact
COLLEEN BOSWELL
Other 510(k) Applications for this Contact
Regulation Number
872.1720
More FDA Info for this Regulation Number
Classification Product Code
EAT
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/24/2002
Decision Date
06/19/2002
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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