IPS E.MAX PRESS MULTI— 510(k) K120134

Substantially Equivalent

Ivoclar Vivadent, AG

FDA 510(k) clearance K120134 for IPS E.MAX PRESS MULTI, Substantially Equivalent on 2012-06-25. Applicant: Ivoclar Vivadent, AG. Device class: 2.

Clearance details

Applicant: Ivoclar Vivadent, AG
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2012-01-17
Decision date: 2012-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, 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.