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DENTRON SENSOR

Page Type
Cleared 510(K)
510(k) Number
K080738
510(k) Type
Traditional
Applicant
Dentron Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
57 days
Submission Type
Summary

DENTRON SENSOR

Page Type
Cleared 510(K)
510(k) Number
K080738
510(k) Type
Traditional
Applicant
Dentron Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
57 days
Submission Type
Summary