KAVO DIAGNODENT— 510(k) DEN990002

Unknown

Kavo America

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

Clearance details

Applicant
Kavo America
Product code
Code NBL
Advisory panel
Dental
Date received
Decision date
Decision
Unknown
Clearance type
Post-NSE
Location
Lake Zurich, IL, US
View on FDA.gov ↗

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