KAVO DIAGNODENT— 510(k) DEN990002

Unknown

Kavo America

FDA 510(k) clearance DEN990002 for KAVO DIAGNODENT, Unknown on 2000-02-22. Applicant: Kavo America. Device class: 2.

Clearance details

Applicant: Kavo America
Product code: Code NBL
Device class: Class 2
Regulation: 21 CFR 872.1745
Advisory panel: Dental
Date received: 1999-07-12
Decision date: 2000-02-22
Decision: Unknown
Clearance type: Post-NSE
Location: Lake Zurich, IL, US

View on FDA.gov ↗

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More clearances from Kavo America

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