XERORADIOGRAPHY 125 SYSTEM - MODIFIED— 510(k) K761022

Name: FDA 510(k) clearance K761022
Creator: U.S. Food and Drug Administration
Published: 1976-11-24

Substantially Equivalent

Xeroradiography

FDA 510(k) clearance K761022 for XERORADIOGRAPHY 125 SYSTEM - MODIFIED, Substantially Equivalent on 1976-11-24. Applicant: Xeroradiography. Device class: 2.

Clearance details

Applicant: Xeroradiography
Product code: Code IXK
Device class: Class 2
Regulation: 21 CFR 892.1630
Advisory panel: Radiology
Date received: 1976-11-11
Decision date: 1976-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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