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FDA 510(k)

CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY

K-Number: K802894 · 1981-02-19

ApplicantCordis Corp.
Decision Date1981-02-19
Product CodeFJI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1981-02-19 under 510(k) number K802894. 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 CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY?

CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY is a medical device that received FDA 510(k) clearance on 1981-02-19. The listed applicant is Cordis Corp.. The 510(k) number is K802894.

When did CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY receive FDA 510(k) clearance?

CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY received FDA 510(k) clearance on 1981-02-19, under 510(k) number K802894.

Who is the listed applicant for CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY?

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 DOW C-DAK 1.8MRC ARTIFIC-KIDNEY?

The FDA product code for CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY is FJI.

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Other records listing Cordis Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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