U-FLOAT VALVE 2D9023
K-Number: K781467 · 1978-09-07
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Device Summary
Frequently Asked Questions
What is the U-FLOAT VALVE 2D9023?
U-FLOAT VALVE 2D9023 is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K781467.
When did U-FLOAT VALVE 2D9023 receive FDA 510(k) clearance?
U-FLOAT VALVE 2D9023 received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781467.
Who is the listed applicant for U-FLOAT VALVE 2D9023?
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 U-FLOAT VALVE 2D9023?
The FDA product code for U-FLOAT VALVE 2D9023 is CAF.
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.
Related Devices (Code: CAF)
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.
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