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FDA 510(k)

CATHETER CONNECTOR

K-Number: K023690 · 2003-02-28

ApplicantWorld Metals, Inc.
Decision Date2003-02-28
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is World Metals, Inc.. It received FDA 510(k) clearance on 2003-02-28 under 510(k) number K023690. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER CONNECTOR?

CATHETER CONNECTOR is a medical device that received FDA 510(k) clearance on 2003-02-28. The listed applicant is World Metals, Inc.. The 510(k) number is K023690.

When did CATHETER CONNECTOR receive FDA 510(k) clearance?

CATHETER CONNECTOR received FDA 510(k) clearance on 2003-02-28, under 510(k) number K023690.

Who is the listed applicant for CATHETER CONNECTOR?

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

What is the FDA product code for CATHETER CONNECTOR?

The FDA product code for CATHETER CONNECTOR is KNY.

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Related Devices (Code: KNY)

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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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