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FDA 510(k)

DUAL LUMEN NEEDLE

K-Number: K833308 · 1983-12-27

ApplicantQuinton, Inc.
Decision Date1983-12-27
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUAL LUMEN NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833308. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL LUMEN NEEDLE?

DUAL LUMEN NEEDLE is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Quinton, Inc.. The 510(k) number is K833308.

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

DUAL LUMEN NEEDLE received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833308.

Who is the listed applicant for DUAL LUMEN NEEDLE?

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 DUAL LUMEN NEEDLE?

The FDA product code for DUAL LUMEN NEEDLE is KOC.

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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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