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MULTILINK

Page Type
Cleared 510(K)
510(k) Number
K032470
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
86 days
Submission Type
Statement

MULTILINK

Page Type
Cleared 510(K)
510(k) Number
K032470
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
86 days
Submission Type
Statement