CoreLite X-Ray Specimen Cabinet— 510(k) K193317

Name: FDA 510(k) clearance K193317
Creator: U.S. Food and Drug Administration
Published: 2019-12-13

Substantially Equivalent

Cirdan Imaging Limited

FDA 510(k) clearance K193317 for CoreLite X-Ray Specimen Cabinet, Substantially Equivalent on 2019-12-13. Applicant: Cirdan Imaging Limited. Device class: 2.

Clearance details

Applicant: Cirdan Imaging Limited
Product code: Code MWP
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2019-11-29
Decision date: 2019-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lisburn, GB

Download summary PDF View on FDA.gov ↗

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