Shimadzu X-Ray High Voltage Generator UD150B

FDA 510(k) K884477 · Shimadzu Precision Instruments, Inc.

Substantially Equivalent

510(k) numberK884477

Submission

Device name
Shimadzu X-Ray High Voltage Generator UD150B
Applicant
Shimadzu Precision Instruments, Inc.
Torrance, CA, US
Received
October 25, 1988
Decision date
March 15, 1989
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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More from Dk Medical Systems Co., Ltd.

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K884598Shimadzu Digital Subtraction System DAR-1200JAA · Traditional 04/20/1989SE
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 X-Ray High Voltage Generator UD150B cleared by the FDA?

Shimadzu X-Ray High Voltage Generator UD150B (K884477) received a 510(k) decision of Substantially Equivalent on March 15, 1989, 141 days after the submission was received.

What is the product code of K884477?

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