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BLUEPHASE 20I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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