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FDA 510(k)

URINARY DRAINAGE BAG 2D9017

K-Number: K772113 · 1977-11-16

Decision Date1977-11-16
Product CodeEYZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY DRAINAGE BAG 2D9017 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1977-11-16 under 510(k) number K772113. The device is classified under product code EYZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY DRAINAGE BAG 2D9017?

URINARY DRAINAGE BAG 2D9017 is a medical device that received FDA 510(k) clearance on 1977-11-16. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K772113.

When did URINARY DRAINAGE BAG 2D9017 receive FDA 510(k) clearance?

URINARY DRAINAGE BAG 2D9017 received FDA 510(k) clearance on 1977-11-16, under 510(k) number K772113.

Who is the listed applicant for URINARY DRAINAGE BAG 2D9017?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINARY DRAINAGE BAG 2D9017?

The FDA product code for URINARY DRAINAGE BAG 2D9017 is EYZ.

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 Travenol Laboratories, S.A. 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 206 devices →

Related Devices (Code: EYZ)

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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