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FDA 510(k)

CLIRANS MODEL TAF 15 HOLLOW FIBER

K-Number: K833503 · 1983-12-08

Decision Date1983-12-08
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLIRANS MODEL TAF 15 HOLLOW FIBER 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 1983-12-08 under 510(k) number K833503. 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 MODEL TAF 15 HOLLOW FIBER?

CLIRANS MODEL TAF 15 HOLLOW FIBER is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Terumo Medical Corp.. The 510(k) number is K833503.

When did CLIRANS MODEL TAF 15 HOLLOW FIBER receive FDA 510(k) clearance?

CLIRANS MODEL TAF 15 HOLLOW FIBER received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833503.

Who is the listed applicant for CLIRANS MODEL TAF 15 HOLLOW FIBER?

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 MODEL TAF 15 HOLLOW FIBER?

The FDA product code for CLIRANS MODEL TAF 15 HOLLOW FIBER is KOC.

Related Clinical Trials

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.

Other records listing Terumo Medical 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.

View all 143 devices →

Related Devices (Code: KOC)

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.

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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