Model MS-325 Radiographic X-Ray Generator

FDA 510(k) K860025 · Medicor USA , Ltd.

Substantially Equivalent

510(k) numberK860025

Submission

Device name
Model MS-325 Radiographic X-Ray Generator
Applicant
Medicor USA , Ltd.
Columbus, OH, US
Received
January 3, 1986
Decision date
May 7, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KPR – System, X-Ray, Stationary
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1680
Specialty
Radiology

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K850761Model Pcx/Emy 525A Microprocesssor Control X-Ray CBZN · Traditional 09/19/1985SE
K851358Model Bion 2/TYPE 90 Room IonizerFRF · Traditional 07/01/1985SE
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K843335Floor Mounted X-Ray TubestandIYB · Traditional 11/27/1984SE
K840227UROLIX-3 Urological TableIXR · Traditional 03/23/1984SE
K840225C-Arm Ceiling Crane FT-2JAA · Traditional 03/22/1984SE
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K823695CPM Metabolic MonitorBZL · Traditional 01/14/1983SE

Questions and answers

When was Model MS-325 Radiographic X-Ray Generator cleared by the FDA?

Model MS-325 Radiographic X-Ray Generator (K860025) received a 510(k) decision of Substantially Equivalent on May 7, 1986, 124 days after the submission was received.

What is the product code of K860025?

The FDA product code is KPR – System, X-Ray, Stationary, a Class II (moderate risk) device regulated under 21 CFR 892.1680.