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FDA 510(k)

ARROW VESSEL CATHETER. KIT W/20GA INDWEL

K-Number: K810962 · 1981-04-29

ApplicantArrow Intl., Inc.
Decision Date1981-04-29
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW VESSEL CATHETER. KIT W/20GA INDWEL 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 1981-04-29 under 510(k) number K810962. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW VESSEL CATHETER. KIT W/20GA INDWEL?

ARROW VESSEL CATHETER. KIT W/20GA INDWEL is a medical device that received FDA 510(k) clearance on 1981-04-29. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K810962.

When did ARROW VESSEL CATHETER. KIT W/20GA INDWEL receive FDA 510(k) clearance?

ARROW VESSEL CATHETER. KIT W/20GA INDWEL received FDA 510(k) clearance on 1981-04-29, under 510(k) number K810962.

Who is the listed applicant for ARROW VESSEL CATHETER. KIT W/20GA INDWEL?

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 VESSEL CATHETER. KIT W/20GA INDWEL?

The FDA product code for ARROW VESSEL CATHETER. KIT W/20GA INDWEL is DQY.

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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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