Apoller Flow Light Cure Flowable Composite— 510(k) K180463

Name: FDA 510(k) clearance K180463
Creator: U.S. Food and Drug Administration
Published: 2018-11-14

Substantially Equivalent

Greenway Yw, LLC

FDA 510(k) clearance K180463 for Apoller Flow Light Cure Flowable Composite, Substantially Equivalent on 2018-11-14. Applicant: Greenway Yw, LLC. Device class: 2.

Clearance details

Applicant: Greenway Yw, LLC
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2018-02-21
Decision date: 2018-11-14
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Lake Bluff, 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.