CURA COMPENSATOR— 510(k) K131150

Name: FDA 510(k) clearance K131150
Creator: U.S. Food and Drug Administration
Published: 2013-07-30

Substantially Equivalent

Cura Medical Technologies, LLC

FDA 510(k) clearance K131150 for CURA COMPENSATOR, Substantially Equivalent on 2013-07-30. 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: 2013-04-23
Decision date: 2013-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, CA, US

Download summary PDF View on FDA.gov ↗

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