ISOPLAST— 510(k) K781787

Substantially Equivalent

Vivadent (Usa), Inc.

FDA 510(k) clearance K781787 for ISOPLAST, Substantially Equivalent on 1978-12-20. Applicant: Vivadent (Usa), Inc..

Clearance details

Applicant: Vivadent (Usa), Inc.
Product code: Code EBF
Advisory panel: Dental
Date received: 1978-10-19
Decision date: 1978-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.