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FDA 510(k)

CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR

K-Number: K921936 · 1992-10-30

ApplicantCordis Corp.
Decision Date1992-10-30
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1992-10-30 under 510(k) number K921936. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR?

CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR is a medical device that received FDA 510(k) clearance on 1992-10-30. The listed applicant is Cordis Corp.. The 510(k) number is K921936.

When did CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR receive FDA 510(k) clearance?

CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR received FDA 510(k) clearance on 1992-10-30, under 510(k) number K921936.

Who is the listed applicant for CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR?

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

What is the FDA product code for CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR?

The FDA product code for CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR is JXG.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: JXG)

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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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