FDA 510(k)

CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER

K-Number: K911703 · 1991-06-28

Decision Date1991-06-28

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING 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 1991-06-28 under 510(k) number K911703. 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 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER?

CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1991-06-28. The listed applicant is Cordis Corp.. The 510(k) number is K911703.

When did CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER receive FDA 510(k) clearance?

CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER received FDA 510(k) clearance on 1991-06-28, under 510(k) number K911703.

Who is the listed applicant for CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING 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 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER?

The FDA product code for CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING 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.