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TRIPLE-CURE PASTE/PASTE RESIN-REINFORCED GLASS IONOMER CEMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030036
510(k) Type
Traditional
Applicant
PULPDENT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2003
Days to Decision
68 days
Submission Type
Summary

TRIPLE-CURE PASTE/PASTE RESIN-REINFORCED GLASS IONOMER CEMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030036
510(k) Type
Traditional
Applicant
PULPDENT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2003
Days to Decision
68 days
Submission Type
Summary