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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 the device name listed in this FDA 510(k) record. The listed applicant is Centurion Medical Products. It received FDA 510(k) clearance on 2022-05-17 under 510(k) 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. The listed applicant is Centurion Medical Products. The 510(k) number is K210548.

When did Medline Integrated Arterial Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Medline Integrated Arterial Catheter?

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

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

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

Other records listing Centurion Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: DQX)

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Official Source

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

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