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FDA 510(k)

ARROW BLOOD CONTAINMENT DEVICE

K-Number: K924558 · 1993-08-19

ApplicantArrow Intl., Inc.
Decision Date1993-08-19
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW BLOOD CONTAINMENT DEVICE 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 1993-08-19 under 510(k) number K924558. 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 BLOOD CONTAINMENT DEVICE?

ARROW BLOOD CONTAINMENT DEVICE is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K924558.

When did ARROW BLOOD CONTAINMENT DEVICE receive FDA 510(k) clearance?

ARROW BLOOD CONTAINMENT DEVICE received FDA 510(k) clearance on 1993-08-19, under 510(k) number K924558.

Who is the listed applicant for ARROW BLOOD CONTAINMENT DEVICE?

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 BLOOD CONTAINMENT DEVICE?

The FDA product code for ARROW BLOOD CONTAINMENT DEVICE is DQX.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: 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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