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RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT

Page Type
Cleared 510(K)
510(k) Number
K042215
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2004
Days to Decision
36 days
Submission Type
Statement

RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT

Page Type
Cleared 510(K)
510(k) Number
K042215
510(k) Type
Traditional
Applicant
PREMIER DENTAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2004
Days to Decision
36 days
Submission Type
Statement