FDA 510(k)

CORDIS ANGIOGRAPHIC DOPPLER CATHER

K-Number: K915498 · 1992-04-17

Decision Date1992-04-17

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS ANGIOGRAPHIC DOPPLER CATHER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1992-04-17 under 510(k) number K915498. 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 ANGIOGRAPHIC DOPPLER CATHER?

CORDIS ANGIOGRAPHIC DOPPLER CATHER is a medical device that received FDA 510(k) clearance on 1992-04-17. The listed applicant is Cordis Corp.. The 510(k) number is K915498.

When did CORDIS ANGIOGRAPHIC DOPPLER CATHER receive FDA 510(k) clearance?

CORDIS ANGIOGRAPHIC DOPPLER CATHER received FDA 510(k) clearance on 1992-04-17, under 510(k) number K915498.

Who is the listed applicant for CORDIS ANGIOGRAPHIC DOPPLER CATHER?

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 ANGIOGRAPHIC DOPPLER CATHER?

The FDA product code for CORDIS ANGIOGRAPHIC DOPPLER CATHER 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.