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FDA 510(k) Application Details - K071192
Device Classification Name
Material, Impression
More FDA Info for this Device
510(K) Number
K071192
Device Name
Material, Impression
Applicant
LANCER ORTHODONTICS, INC.
3722 AVE. SAUSALITO
IRVINE, CA 92606 US
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Contact
GRACE HOLLAND
Other 510(k) Applications for this Contact
Regulation Number
872.3660
More FDA Info for this Regulation Number
Classification Product Code
ELW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/30/2007
Decision Date
06/22/2007
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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