MODIFICATION TO WBR, MODEL HR— 510(k) K031874

Name: FDA 510(k) clearance K031874
Creator: U.S. Food and Drug Administration
Published: 2003-07-18

Substantially Equivalent

U.C.G. Technologies , Ltd.

FDA 510(k) clearance K031874 for MODIFICATION TO WBR, MODEL HR, Substantially Equivalent on 2003-07-18. Applicant: U.C.G. Technologies , Ltd.. Device class: 2.

Clearance details

Applicant: U.C.G. Technologies , Ltd.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 2003-06-17
Decision date: 2003-07-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Haifa, IL

Download summary PDF View on FDA.gov ↗

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