FDA 510(k)

CORDIS CONTRAST INJECTION LINES

K-Number: K864141 · 1986-11-03

Decision Date1986-11-03

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS CONTRAST INJECTION LINES is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-11-03 under 510(k) number K864141. 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 CONTRAST INJECTION LINES?

CORDIS CONTRAST INJECTION LINES is a medical device that received FDA 510(k) clearance on 1986-11-03. The listed applicant is Cordis Corp.. The 510(k) number is K864141.

When did CORDIS CONTRAST INJECTION LINES receive FDA 510(k) clearance?

CORDIS CONTRAST INJECTION LINES received FDA 510(k) clearance on 1986-11-03, under 510(k) number K864141.

Who is the listed applicant for CORDIS CONTRAST INJECTION LINES?

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 CONTRAST INJECTION LINES?

The FDA product code for CORDIS CONTRAST INJECTION LINES 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.