HEMOSIL LIQUID ANTITHROMBIN
K-Number: K062431 · 2006-09-01
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Device Summary
Frequently Asked Questions
What is the HEMOSIL LIQUID ANTITHROMBIN?
HEMOSIL LIQUID ANTITHROMBIN is a medical device that received FDA 510(k) clearance on 2006-09-01. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K062431.
When did HEMOSIL LIQUID ANTITHROMBIN receive FDA 510(k) clearance?
HEMOSIL LIQUID ANTITHROMBIN received FDA 510(k) clearance on 2006-09-01, under 510(k) number K062431.
Who is the listed applicant for HEMOSIL LIQUID ANTITHROMBIN?
The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMOSIL LIQUID ANTITHROMBIN?
The FDA product code for HEMOSIL LIQUID ANTITHROMBIN is JBQ.
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 Instrumentation Laboratory CO 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: JBQ)
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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