Rainbow 360— 510(k) K222830

Substantially Equivalent

Kerr Corporation

FDA 510(k) clearance K222830 for Rainbow 360, Substantially Equivalent on 2023-01-12. Applicant: Kerr Corporation. Device class: 2.

Clearance details

Applicant: Kerr Corporation
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2022-09-19
Decision date: 2023-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pomona, CA, 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.