PIEZOMED— 510(k) K133488

Substantially Equivalent

W&H Dentalwerk Buermoos GmbH

FDA 510(k) clearance K133488 for PIEZOMED, Substantially Equivalent on 2014-10-16. Applicant: W&H Dentalwerk Buermoos GmbH. Device class: 2.

Clearance details

Applicant: W&H Dentalwerk Buermoos GmbH
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2013-11-13
Decision date: 2014-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burmoos, AT

Download summary PDF View on FDA.gov ↗

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