IONOFIL PLUS AC— 510(k) K042669

Substantially Equivalent

Voco GmbH

FDA 510(k) clearance K042669 for IONOFIL PLUS AC, Substantially Equivalent on 2004-10-20. Applicant: Voco GmbH. Device class: 2.

Clearance details

Applicant: Voco GmbH
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2004-09-29
Decision date: 2004-10-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Bend, OR, 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.