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FDA 510(k)

ulrichINJECT CT motion

K-Number: K210541 · 2021-08-06

ApplicantUlrich GmbH & Co. KG
Decision Date2021-08-06
Product CodeIZQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ulrichINJECT CT motion is a medical device manufactured by Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2021-08-06 under approval number K210541. The device is classified under product code IZQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ulrichINJECT CT motion?

ulrichINJECT CT motion is a medical device that received FDA 510(k) clearance on 2021-08-06. It is manufactured by Ulrich GmbH & Co. KG. The 510(k) number is K210541.

When was ulrichINJECT CT motion approved by the FDA?

ulrichINJECT CT motion received FDA 510(k) clearance on 2021-08-06, under approval number K210541.

What company makes ulrichINJECT CT motion?

ulrichINJECT CT motion is manufactured by Ulrich GmbH & Co. KG.

What is the FDA product code for ulrichINJECT CT motion?

The FDA product code for ulrichINJECT CT motion is IZQ.

Other Devices by Ulrich GmbH & Co. KG

K161032neon3™ universal OCT spinal stabilization K161723ulrich Transfer Set K171392ulrichINJECT CT motion K192117Small VBR™ K202227Artus™ cervical plate system K192872ulrichINJECT CT Motion

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Related Devices (Code: IZQ)

K151048CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient SetBracco Injeneering K152361OptiOne Single-Head Contrast Delivery System with Pedestal; with Ceiling Suspension;Injector, OptiOne Base SystemLiebel-Flarsheim Company, LLC K171392ulrichINJECT CT motionUlrich GmbH & Co. KG K192872ulrichINJECT CT MotionUlrich GmbH & Co. KG K241849MEDRAD Centargo CT Injection System; MEDRAD Centargo Day Set; MEDRAD Centargo Patient Line; MEDRAD Centargo Replacement Spike; MEDRAD ISI2 Module (ISI2)Imaxeon Pty, Ltd. K241850ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)Ulrich GmbH & Co. KG

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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