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AMERICAN DENTAL PRODUCTS LIGHT ACTIVATED COMPOSITE RESIN CORE BUILDUP BLUE PASTEE

Page Type
Cleared 510(K)
510(k) Number
K954408
510(k) Type
Traditional
Applicant
AMERICAN DENTAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1995
Days to Decision
40 days
Submission Type
Summary

AMERICAN DENTAL PRODUCTS LIGHT ACTIVATED COMPOSITE RESIN CORE BUILDUP BLUE PASTEE

Page Type
Cleared 510(K)
510(k) Number
K954408
510(k) Type
Traditional
Applicant
AMERICAN DENTAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1995
Days to Decision
40 days
Submission Type
Summary