U.S.I. MODEL 1012, REMOTE FLUOROSCOPIC CONTROL— 510(k) K900062

Name: FDA 510(k) clearance K900062
Creator: U.S. Food and Drug Administration
Published: 1990-02-05

Substantially Equivalent

U.S. Imaging, Inc.

FDA 510(k) clearance K900062 for U.S.I. MODEL 1012, REMOTE FLUOROSCOPIC CONTROL, Substantially Equivalent on 1990-02-05. Applicant: U.S. Imaging, Inc.. Device class: 1.

Clearance details

Applicant: U.S. Imaging, Inc.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1990-01-03
Decision date: 1990-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greensburg, OH, US

Download summary PDF View on FDA.gov ↗

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