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FDA 510(k)

EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR

K-Number: K823733 · 1983-01-14

ApplicantAdvocacy International, Ltd.
Decision Date1983-01-14
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR is the device name listed in this FDA 510(k) record. The listed applicant is Advocacy International, Ltd.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823733. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR?

EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Advocacy International, Ltd.. The 510(k) number is K823733.

When did EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR receive FDA 510(k) clearance?

EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823733.

Who is the listed applicant for EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR?

The FDA 510(k) record lists Advocacy International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR?

The FDA product code for EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR is KOC.

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Related Devices (Code: KOC)

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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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