Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K121230
Device Classification Name
Material, Tooth Shade, Resin
More FDA Info for this Device
510(K) Number
K121230
Device Name
Material, Tooth Shade, Resin
Applicant
IVOCLAR VIVADENT AG
BENDERERSTRASSE 2
SCHAAN FL-9494 LI
Other 510(k) Applications for this Company
Contact
SANDRA CAKEBREAD
Other 510(k) Applications for this Contact
Regulation Number
872.3690
More FDA Info for this Regulation Number
Classification Product Code
EBF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/24/2012
Decision Date
08/29/2012
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact