FDA 510(k)

CORDIS 7 FRENCH THRULUMEN CATHETER

K-Number: K922891 · 1993-06-23

Decision Date1993-06-23

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS 7 FRENCH THRULUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1993-06-23 under 510(k) number K922891. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS 7 FRENCH THRULUMEN CATHETER?

CORDIS 7 FRENCH THRULUMEN CATHETER is a medical device that received FDA 510(k) clearance on 1993-06-23. The listed applicant is Cordis Corp.. The 510(k) number is K922891.

When did CORDIS 7 FRENCH THRULUMEN CATHETER receive FDA 510(k) clearance?

CORDIS 7 FRENCH THRULUMEN CATHETER received FDA 510(k) clearance on 1993-06-23, under 510(k) number K922891.

Who is the listed applicant for CORDIS 7 FRENCH THRULUMEN CATHETER?

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 7 FRENCH THRULUMEN CATHETER?

The FDA product code for CORDIS 7 FRENCH THRULUMEN CATHETER is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.