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DENTOETCH QUICKBOND BOND ACTIVATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122522
510(k) Type
Traditional
Applicant
Itena Clinical
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/19/2013
Days to Decision
211 days
Submission Type
Summary

DENTOETCH QUICKBOND BOND ACTIVATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122522
510(k) Type
Traditional
Applicant
Itena Clinical
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/19/2013
Days to Decision
211 days
Submission Type
Summary