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FDA 510(k)

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW

K-Number: K761007 · 1977-01-12

ApplicantCordis Corp.
Decision Date1977-01-12
Product CodeFJI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K761007. The device is classified under product code FJI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTIFICIAL KIDNEY, C-DAK CORDIS DOW?

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Cordis Corp.. The 510(k) number is K761007.

When did ARTIFICIAL KIDNEY, C-DAK CORDIS DOW receive FDA 510(k) clearance?

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW received FDA 510(k) clearance on 1977-01-12, under 510(k) number K761007.

Who is the listed applicant for ARTIFICIAL KIDNEY, C-DAK CORDIS DOW?

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 ARTIFICIAL KIDNEY, C-DAK CORDIS DOW?

The FDA product code for ARTIFICIAL KIDNEY, C-DAK CORDIS DOW is FJI.

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Other records listing Cordis Corp. as applicant

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K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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Related Devices (Code: FJI)

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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.

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