KAVO INTRASEPT 905— 510(k) K934783

Substantially Equivalent

Kavo America

FDA 510(k) clearance K934783 for KAVO INTRASEPT 905, Substantially Equivalent on 1994-05-16. Applicant: Kavo America. Device class: 1.

Clearance details

Applicant: Kavo America
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1993-10-06
Decision date: 1994-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Zurich, IL, 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.