CURA COLLIMATOR— 510(k) K123893

Substantially Equivalent

Cura Medical Technologies, LLC

FDA 510(k) clearance K123893 for CURA COLLIMATOR, Substantially Equivalent on 2013-03-04. Applicant: Cura Medical Technologies, LLC. Device class: 2.

Clearance details

Applicant: Cura Medical Technologies, LLC
Product code: Code IXI
Device class: Class 2
Regulation: 21 CFR 892.5710
Advisory panel: Radiology
Date received: 2012-12-18
Decision date: 2013-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, 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.