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FDA 510(k)

TUBING ORGANIZER

K-Number: K895706 · 1989-10-31

Decision Date1989-10-31
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBING ORGANIZER is the device name listed in this FDA 510(k) record. The listed applicant is 3t Products, Inc.. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K895706. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING ORGANIZER?

TUBING ORGANIZER is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is 3t Products, Inc.. The 510(k) number is K895706.

When did TUBING ORGANIZER receive FDA 510(k) clearance?

TUBING ORGANIZER received FDA 510(k) clearance on 1989-10-31, under 510(k) number K895706.

Who is the listed applicant for TUBING ORGANIZER?

The FDA 510(k) record lists 3t Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUBING ORGANIZER?

The FDA product code for TUBING ORGANIZER is KNT.

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.

Related Devices (Code: KNT)

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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