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PRIME-DENT HEMA DESENSITIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013970
510(k) Type
Traditional
Applicant
PRIME DENTAL MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
78 days
Submission Type
Statement

PRIME-DENT HEMA DESENSITIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013970
510(k) Type
Traditional
Applicant
PRIME DENTAL MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2002
Days to Decision
78 days
Submission Type
Statement