Shimadzu Digital Subtraction System DAR-1200

FDA 510(k) K884598 · Shimadzu Precision Instruments, Inc.

Substantially Equivalent

510(k) numberK884598

Submission

Device name
Shimadzu Digital Subtraction System DAR-1200
Applicant
Shimadzu Precision Instruments, Inc.
Torrance, CA, US
Received
November 3, 1988
Decision date
April 20, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

Other 510(k)s with product code JAA

510(k)DeviceApplicantDecision
K253103Nexus DRF Digital X-ray Imaging SystemJAA · Traditional Varex Imaging Corporation05/29/2026SE
K251650Insight Enhanced™ DRF (EN-1002-01)JAA · Traditional Imaging Engineering, LLC09/16/2025SE
K242488Soteria E-ViewJAA · Traditional Omega Medical Imaging, LLC01/06/2025SE
K242948Adora DRFi (04550010)JAA · Traditional Nrt X-Ray A/S12/23/2024SE
K233380TRIDENT Mobile Fluoroscopy SystemJAA · Traditional Dornier Medtech America06/26/2024SE
K233945ProxiDiagnost N90 / Precision CRF (706110, 706400)JAA · Special Philips Medical Systems Dmc GmbH01/11/2024SE
K232910CombiDiagnost R90JAA · Special Philips Medical Systems Dmc GmbH10/19/2023SE
K232526XIDF-AWS801, Angio Workstation (Alphenix Workstation), V9.5JAA · Special Canon Medical Systems Corporation09/12/2023SE
K220871NautilusJAA · Special Dornier Medtech America, Inc.04/18/2022SE
K212890Nyquist.IQJAA · Traditional Omega Medical Imaging, LLC12/13/2021SE

More from Omega Medical Imaging, LLC

510(k)DeviceDecision
K940294Shimadzu Mobile X-Ray SystemsOXO · Traditional 03/16/1994SE
K890913Sdu 800 Diagnostic Ultrasound InstrumentIYO · Traditional 09/06/1989SE
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 Digital Subtraction System DAR-1200 cleared by the FDA?

Shimadzu Digital Subtraction System DAR-1200 (K884598) received a 510(k) decision of Substantially Equivalent on April 20, 1989, 168 days after the submission was received.

What is the product code of K884598?

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