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FDA 510(k)

GREEN CROSS URINARY DRAINAGE BAG

K-Number: K843117 · 1984-10-11

Decision Date1984-10-11
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GREEN CROSS URINARY DRAINAGE BAG is the device name listed in this FDA 510(k) record. The listed applicant is Tech-Cons Ltd., Intl.. It received FDA 510(k) clearance on 1984-10-11 under 510(k) number K843117. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREEN CROSS URINARY DRAINAGE BAG?

GREEN CROSS URINARY DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1984-10-11. The listed applicant is Tech-Cons Ltd., Intl.. The 510(k) number is K843117.

When did GREEN CROSS URINARY DRAINAGE BAG receive FDA 510(k) clearance?

GREEN CROSS URINARY DRAINAGE BAG received FDA 510(k) clearance on 1984-10-11, under 510(k) number K843117.

Who is the listed applicant for GREEN CROSS URINARY DRAINAGE BAG?

The FDA 510(k) record lists Tech-Cons Ltd., Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREEN CROSS URINARY DRAINAGE BAG?

The FDA product code for GREEN CROSS URINARY DRAINAGE BAG is KNX.

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 Tech-Cons Ltd., Intl. 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.

Related Devices (Code: KNX)

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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