VIVASENS— 510(k) K030922

Substantially Equivalent

Ivoclar Vivadent, Inc.

FDA 510(k) clearance K030922 for VIVASENS, Substantially Equivalent on 2003-10-17. Applicant: Ivoclar Vivadent, Inc..

Clearance details

Applicant: Ivoclar Vivadent, Inc.
Product code: Code LBH
Advisory panel: Dental
Date received: 2003-03-24
Decision date: 2003-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

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