Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ulrichINJECT CT Motion

K-Number: K192872 · 2020-07-02

Decision Date2020-07-02
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 2020-07-02 under approval number K192872. 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 2020-07-02. It is manufactured by Ulrich GmbH & Co. KG. The 510(k) number is K192872.

When was ulrichINJECT CT Motion approved by the FDA?

ulrichINJECT CT Motion received FDA 510(k) clearance on 2020-07-02, under approval number K192872.

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

View all 11 devices →

Related Devices (Code: IZQ)

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.