MOTORIZED MICRO MULTILEAF COLLIMATOR— 510(k) K000349

Name: FDA 510(k) clearance K000349
Creator: U.S. Food and Drug Administration
Published: 2000-05-03

Substantially Equivalent

Stryker Leibinger

FDA 510(k) clearance K000349 for MOTORIZED MICRO MULTILEAF COLLIMATOR, Substantially Equivalent on 2000-05-03. Applicant: Stryker Leibinger. Device class: 2.

Clearance details

Applicant: Stryker Leibinger
Product code: Code IXI
Device class: Class 2
Regulation: 21 CFR 892.5710
Advisory panel: Radiology
Date received: 2000-02-03
Decision date: 2000-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, 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.