ORTHOCAD IQ— 510(k) K082207

Substantially Equivalent

Cadent, Inc.

FDA 510(k) clearance K082207 for ORTHOCAD IQ, Substantially Equivalent on 2009-10-23. Applicant: Cadent, Inc.. Device class: 2.

Clearance details

Applicant: Cadent, Inc.
Product code: Code DYW
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2008-08-05
Decision date: 2009-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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