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PERMAQUIK BONDING PRIMER

Page Type
Cleared 510(K)
510(k) Number
K951583
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1995
Days to Decision
36 days
Submission Type
Statement

PERMAQUIK BONDING PRIMER

Page Type
Cleared 510(K)
510(k) Number
K951583
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1995
Days to Decision
36 days
Submission Type
Statement