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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 the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-04-30 under 510(k) 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. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K220243.

When did Ultiri Measurement System receive FDA 510(k) clearance?

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

Who is the listed applicant for Ultiri Measurement System?

The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: DQK)

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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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