FDA 510(k)

DOUBLE LUMEN CATHETER

K-Number: K872248 · 1987-08-12

Decision Date1987-08-12

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DOUBLE LUMEN 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 1987-08-12 under 510(k) number K872248. 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 DOUBLE LUMEN CATHETER?

DOUBLE LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 1987-08-12. The listed applicant is Cordis Corp.. The 510(k) number is K872248.

When did DOUBLE LUMEN CATHETER receive FDA 510(k) clearance?

DOUBLE LUMEN CATHETER received FDA 510(k) clearance on 1987-08-12, under 510(k) number K872248.

Who is the listed applicant for DOUBLE LUMEN 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 DOUBLE LUMEN CATHETER?

The FDA product code for DOUBLE LUMEN CATHETER is DQO.

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Other records listing Cordis Corp. as applicant

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER K101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE K082143MICRO GUIDE CATHETER XP K062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MB K060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAX K050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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.