LIBERTY VALVE
K-Number: K964690 · 1997-03-21
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Device Summary
Frequently Asked Questions
What is the LIBERTY VALVE?
LIBERTY VALVE is a medical device that received FDA 510(k) clearance on 1997-03-21. The listed applicant is Cleveland Medical Devices, Inc.. The 510(k) number is K964690.
When did LIBERTY VALVE receive FDA 510(k) clearance?
LIBERTY VALVE received FDA 510(k) clearance on 1997-03-21, under 510(k) number K964690.
Who is the listed applicant for LIBERTY VALVE?
The FDA 510(k) record lists Cleveland Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIBERTY VALVE?
The FDA product code for LIBERTY VALVE 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 Cleveland Medical Devices, 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: 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
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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