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DENTINSENSE B/C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965138
510(k) Type
Traditional
Applicant
CENTRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1997
Days to Decision
53 days
Submission Type
Statement

DENTINSENSE B/C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965138
510(k) Type
Traditional
Applicant
CENTRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1997
Days to Decision
53 days
Submission Type
Statement