DIGORA FOR WINDOWS 2.0— 510(k) K983267

Name: FDA 510(k) clearance K983267
Creator: U.S. Food and Drug Administration
Published: 1998-12-30

Substantially Equivalent

Orion Corporation Soredex

FDA 510(k) clearance K983267 for DIGORA FOR WINDOWS 2.0, Substantially Equivalent on 1998-12-30. Applicant: Orion Corporation Soredex. Device class: 2.

Clearance details

Applicant: Orion Corporation Soredex
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1998-09-17
Decision date: 1998-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, FI

Download summary PDF View on FDA.gov ↗

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