FDA 510(k)

CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER

K-Number: K914141 · 1991-10-23

Decision Date1991-10-23

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS DUAL LUMEN PRESSURE MONITORING 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 1991-10-23 under 510(k) number K914141. 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 DUAL LUMEN PRESSURE MONITORING CATHETER?

CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Cordis Corp.. The 510(k) number is K914141.

When did CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER receive FDA 510(k) clearance?

CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER received FDA 510(k) clearance on 1991-10-23, under 510(k) number K914141.

Who is the listed applicant for CORDIS DUAL LUMEN PRESSURE MONITORING 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 DUAL LUMEN PRESSURE MONITORING CATHETER?

The FDA product code for CORDIS DUAL LUMEN PRESSURE MONITORING 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.