LIQUICORD
K-Number: K092384 · 2009-11-04
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Device Summary
Frequently Asked Questions
What is the LIQUICORD?
LIQUICORD is a medical device that received FDA 510(k) clearance on 2009-11-04. The listed applicant is Centrix, Inc.. The 510(k) number is K092384.
When did LIQUICORD receive FDA 510(k) clearance?
LIQUICORD received FDA 510(k) clearance on 2009-11-04, under 510(k) number K092384.
Who is the listed applicant for LIQUICORD?
The FDA 510(k) record lists Centrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUICORD?
The FDA product code for LIQUICORD is MVL.
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 Centrix, 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: MVL)
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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