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FDA 510(k)

ARROW RADIAL ARTERY CATHETERIZATION SET

K-Number: K810675 · 1981-03-27

ApplicantArrow Intl., Inc.
Decision Date1981-03-27
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW RADIAL ARTERY CATHETERIZATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1981-03-27 under 510(k) number K810675. 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 ARROW RADIAL ARTERY CATHETERIZATION SET?

ARROW RADIAL ARTERY CATHETERIZATION SET is a medical device that received FDA 510(k) clearance on 1981-03-27. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K810675.

When did ARROW RADIAL ARTERY CATHETERIZATION SET receive FDA 510(k) clearance?

ARROW RADIAL ARTERY CATHETERIZATION SET received FDA 510(k) clearance on 1981-03-27, under 510(k) number K810675.

Who is the listed applicant for ARROW RADIAL ARTERY CATHETERIZATION SET?

The FDA 510(k) record lists Arrow Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARROW RADIAL ARTERY CATHETERIZATION SET?

The FDA product code for ARROW RADIAL ARTERY CATHETERIZATION SET is DQX.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: DQX)

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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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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