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EXCITE SELF ETCH

Page Type
Cleared 510(K)
510(k) Number
K013584
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2002
Days to Decision
90 days
Submission Type
Statement

EXCITE SELF ETCH

Page Type
Cleared 510(K)
510(k) Number
K013584
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2002
Days to Decision
90 days
Submission Type
Statement