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FDA 510(k)

CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &

K-Number: K831482 · 1983-06-03

ApplicantTerumo Medical Corp.
Decision Date1983-06-03
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLIRANS TAF 120 HOLLOW FIBER DIALYZ. & is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K831482. 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 CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &?

CLIRANS TAF 120 HOLLOW FIBER DIALYZ. & is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Terumo Medical Corp.. The 510(k) number is K831482.

When did CLIRANS TAF 120 HOLLOW FIBER DIALYZ. & receive FDA 510(k) clearance?

CLIRANS TAF 120 HOLLOW FIBER DIALYZ. & received FDA 510(k) clearance on 1983-06-03, under 510(k) number K831482.

Who is the listed applicant for CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &?

The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &?

The FDA product code for CLIRANS TAF 120 HOLLOW FIBER DIALYZ. & is 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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