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PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994181
510(k) Type
Traditional
Applicant
PULPDENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2000
Days to Decision
81 days
Submission Type
Statement

PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994181
510(k) Type
Traditional
Applicant
PULPDENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2000
Days to Decision
81 days
Submission Type
Statement