EXT-600 Table, Radiographic, Elevating

FDA 510(k) K896665 · Rms Div.

Substantially Equivalent

510(k) numberK896665

Submission

Device name
EXT-600 Table, Radiographic, Elevating
Applicant
Rms Div.
Addison, IL, US
Received
November 27, 1989
Decision date
January 22, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IZZ – Table, Radiographic, Non-Tilting, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1980
Specialty
Radiology

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K921501Deluxe C Arm Radiological Table, Model #056-004IZZ · Traditional Biodan Medical Systems, Ltd.05/15/1992SE
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Questions and answers

When was EXT-600 Table, Radiographic, Elevating cleared by the FDA?

EXT-600 Table, Radiographic, Elevating (K896665) received a 510(k) decision of Substantially Equivalent on January 22, 1990, 56 days after the submission was received.

What is the product code of K896665?

The FDA product code is IZZ – Table, Radiographic, Non-Tilting, Powered, a Class II (moderate risk) device regulated under 21 CFR 892.1980.