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ASTRALIS 7, MODEL 557545

Page Type
Cleared 510(K)
510(k) Number
K013277
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2001
Days to Decision
20 days
Submission Type
Statement

ASTRALIS 7, MODEL 557545

Page Type
Cleared 510(K)
510(k) Number
K013277
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2001
Days to Decision
20 days
Submission Type
Statement