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FDA 510(k)

CLIRANS TAF06 HOLLOW FIBER DIALYZER

K-Number: K832252 · 1983-08-26

ApplicantTerumo Medical Corp.
Decision Date1983-08-26
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLIRANS TAF06 HOLLOW FIBER DIALYZER 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 1983-08-26 under 510(k) number K832252. 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 TAF06 HOLLOW FIBER DIALYZER?

CLIRANS TAF06 HOLLOW FIBER DIALYZER is a medical device that received FDA 510(k) clearance on 1983-08-26. The listed applicant is Terumo Medical Corp.. The 510(k) number is K832252.

When did CLIRANS TAF06 HOLLOW FIBER DIALYZER receive FDA 510(k) clearance?

CLIRANS TAF06 HOLLOW FIBER DIALYZER received FDA 510(k) clearance on 1983-08-26, under 510(k) number K832252.

Who is the listed applicant for CLIRANS TAF06 HOLLOW FIBER DIALYZER?

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 TAF06 HOLLOW FIBER DIALYZER?

The FDA product code for CLIRANS TAF06 HOLLOW FIBER DIALYZER 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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