WILLI GELLER CERAMIC CREATION & SURPRISE— 510(k) K900209

Name: FDA 510(k) clearance K900209
Creator: U.S. Food and Drug Administration
Published: 1990-04-09

Substantially Equivalent

Creation North America, Inc.

FDA 510(k) clearance K900209 for WILLI GELLER CERAMIC CREATION & SURPRISE, Substantially Equivalent on 1990-04-09. Applicant: Creation North America, Inc.. Device class: 2.

Clearance details

Applicant: Creation North America, Inc.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 1990-01-17
Decision date: 1990-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, 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.