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BLUEPHASE 20I

Page Type
Cleared 510(K)
510(k) Number
K091020
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2009
Days to Decision
64 days
Submission Type
Statement

BLUEPHASE 20I

Page Type
Cleared 510(K)
510(k) Number
K091020
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2009
Days to Decision
64 days
Submission Type
Statement