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FDA 510(k)

RAAF DUAL LUMEN CATHETER

K-Number: K842176 · 1984-07-13

ApplicantQuinton, Inc.
Decision Date1984-07-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RAAF DUAL LUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1984-07-13 under 510(k) number K842176. 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 RAAF DUAL LUMEN CATHETER?

RAAF DUAL LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 1984-07-13. The listed applicant is Quinton, Inc.. The 510(k) number is K842176.

When did RAAF DUAL LUMEN CATHETER receive FDA 510(k) clearance?

RAAF DUAL LUMEN CATHETER received FDA 510(k) clearance on 1984-07-13, under 510(k) number K842176.

Who is the listed applicant for RAAF DUAL LUMEN CATHETER?

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

What is the FDA product code for RAAF DUAL LUMEN CATHETER?

The FDA product code for RAAF DUAL LUMEN CATHETER 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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