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FDA 510(k)

Ultiri Measurement System

K-Number: K220243 · 2022-04-30

ApplicantABBOTT MEDICAL
Decision Date2022-04-30
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Ultiri Measurement System is a medical device manufactured by ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-04-30 under approval number K220243. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultiri Measurement System?

Ultiri Measurement System is a medical device that received FDA 510(k) clearance on 2022-04-30. It is manufactured by ABBOTT MEDICAL. The 510(k) number is K220243.

When was Ultiri Measurement System approved by the FDA?

Ultiri Measurement System received FDA 510(k) clearance on 2022-04-30, under approval number K220243.

What company makes Ultiri Measurement System?

Ultiri Measurement System is manufactured by ABBOTT MEDICAL.

What is the FDA product code for Ultiri Measurement System?

The FDA product code for Ultiri Measurement System is DQK.

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Related PubMed Literature

PMID: 41336744 From laboratory to pre-market prototyping: lessons learned from a noninvasive blood glucose level measurement device. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference (2025)

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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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