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FDA 510(k)

NON CORING INFUSION SET

K-Number: K881256 · 1988-04-21

ApplicantTaris Corp.
Decision Date1988-04-21
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON CORING INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Taris Corp.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881256. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON CORING INFUSION SET?

NON CORING INFUSION SET is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Taris Corp.. The 510(k) number is K881256.

When did NON CORING INFUSION SET receive FDA 510(k) clearance?

NON CORING INFUSION SET received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881256.

Who is the listed applicant for NON CORING INFUSION SET?

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

What is the FDA product code for NON CORING INFUSION SET?

The FDA product code for NON CORING INFUSION SET is LJT.

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.

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Other records listing Taris 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.

K880887NEOCATHK875153THIELER KIT

Related Devices (Code: LJT)

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.

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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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