REOLIT— 510(k) K802685

Substantially Equivalent

Vivadent (Usa), Inc.

FDA 510(k) clearance K802685 for REOLIT, Substantially Equivalent on 1980-11-12. Applicant: Vivadent (Usa), Inc..

Clearance details

Applicant: Vivadent (Usa), Inc.
Product code: Code EJK
Advisory panel: Dental
Date received: 1980-10-28
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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