Shimadzu Mobile X-Ray Systems

FDA 510(k) K940294 · Shimadzu Precision Instruments, Inc.

Substantially Equivalent

510(k) numberK940294

Submission

Device name
Shimadzu Mobile X-Ray Systems
Applicant
Shimadzu Precision Instruments, Inc.
Torrance, CA, US
Received
January 21, 1994
Decision date
March 16, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
OXO – Image-Intensified Fluoroscopic X-Ray System, Mobile
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1650
Specialty
Radiology

Fluoroscopy of the human body.

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K243452Orthoscan VERSA Mini C-ArmOXO · Traditional Ziehm-Orthoscan, Inc.01/14/2025SE
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More from Ge Oec Medical Systems, Inc.

510(k)DeviceDecision
K890913Sdu 800 Diagnostic Ultrasound InstrumentIYO · Traditional 09/06/1989SE
K884598Shimadzu Digital Subtraction System DAR-1200JAA · Traditional 04/20/1989SE
K884477Shimadzu X-Ray High Voltage Generator UD150BKPR · Traditional 03/15/1989SE
K875378Single Photon Set 031 & AZ-701-NTS-SP EmissionKPS · Traditional 11/16/1988SE
K882311Shimadzu Lateral C-Arm MH-31JAA · Traditional 09/14/1988SE
K881674Shimadzu Whole Body X-Ray CT Scanner SCT-3000TCJAK · Traditional 09/02/1988SE
K881795Shimadzu X-Ray High Voltage Generator UD150KIZO · Traditional 07/01/1988SE
K874910Shimadzu Digital Subtraction System DAR-200IZI · Traditional 07/01/1988SE
K875370Shimadzu Whole Body X-Ray CT Scanner SCT-3000TXJAK · Traditional 05/18/1988SE
K874946Shimadzu X-Ray High Voltage Generator HD150G-60IZO · Traditional 03/03/1988SE

Questions and answers

When was Shimadzu Mobile X-Ray Systems cleared by the FDA?

Shimadzu Mobile X-Ray Systems (K940294) received a 510(k) decision of Substantially Equivalent on March 16, 1994, 54 days after the submission was received.

What is the product code of K940294?

The FDA product code is OXO – Image-Intensified Fluoroscopic X-Ray System, Mobile, a Class II (moderate risk) device regulated under 21 CFR 892.1650.