FDA 510(k)

CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER

K-Number: K921310 · 1992-09-17

Decision Date1992-09-17

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC 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 1992-09-17 under 510(k) number K921310. 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 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER?

CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1992-09-17. The listed applicant is Cordis Corp.. The 510(k) number is K921310.

When did CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1992-09-17, under 510(k) number K921310.

Who is the listed applicant for CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC 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 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER?

The FDA product code for CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC 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.