LEG URINAL
K-Number: K913155 · 1991-09-16
Device Summary
Frequently Asked Questions
What is the LEG URINAL?
LEG URINAL is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Ezmt Valve Co., Inc.. The 510(k) number is K913155.
When did LEG URINAL receive FDA 510(k) clearance?
LEG URINAL received FDA 510(k) clearance on 1991-09-16, under 510(k) number K913155.
Who is the listed applicant for LEG URINAL?
The FDA 510(k) record lists Ezmt Valve Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEG URINAL?
The FDA product code for LEG URINAL is GAQ.
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 Ezmt Valve Co., Inc. 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: GAQ)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.