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SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)

Page Type
Cleared 510(K)
510(k) Number
K003407
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2001
Days to Decision
86 days
Submission Type
Statement

SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)

Page Type
Cleared 510(K)
510(k) Number
K003407
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2001
Days to Decision
86 days
Submission Type
Statement