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FDA 510(k)

Medline Integrated Arterial Catheter

K-Number: K210548 · 2022-05-17

ApplicantCenturion Medical Products
Decision Date2022-05-17
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medline Integrated Arterial Catheter is a medical device manufactured by Centurion Medical Products. It received FDA 510(k) clearance on 2022-05-17 under approval number K210548. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Integrated Arterial Catheter?

Medline Integrated Arterial Catheter is a medical device that received FDA 510(k) clearance on 2022-05-17. It is manufactured by Centurion Medical Products. The 510(k) number is K210548.

When was Medline Integrated Arterial Catheter approved by the FDA?

Medline Integrated Arterial Catheter received FDA 510(k) clearance on 2022-05-17, under approval number K210548.

What company makes Medline Integrated Arterial Catheter?

Medline Integrated Arterial Catheter is manufactured by Centurion Medical Products.

What is the FDA product code for Medline Integrated Arterial Catheter?

The FDA product code for Medline Integrated Arterial Catheter is DQX.

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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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