EUREKA EXTENSION CYLINDERS— 510(k) K904489

Name: FDA 510(k) clearance K904489
Creator: U.S. Food and Drug Administration
Published: 1990-10-15

Substantially Equivalent

Eureka X-Ray Tube Corp.

FDA 510(k) clearance K904489 for EUREKA EXTENSION CYLINDERS, Substantially Equivalent on 1990-10-15. Applicant: Eureka X-Ray Tube Corp.. Device class: 2.

Clearance details

Applicant: Eureka X-Ray Tube Corp.
Product code: Code KPW
Device class: Class 2
Regulation: 21 CFR 892.1610
Advisory panel: Radiology
Date received: 1990-10-02
Decision date: 1990-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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