IL MCL-2 COAGULATION ANALYZER
K-Number: K924098 · 1993-06-18
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Device Summary
Frequently Asked Questions
What is the IL MCL-2 COAGULATION ANALYZER?
IL MCL-2 COAGULATION ANALYZER is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K924098.
When did IL MCL-2 COAGULATION ANALYZER receive FDA 510(k) clearance?
IL MCL-2 COAGULATION ANALYZER received FDA 510(k) clearance on 1993-06-18, under 510(k) number K924098.
Who is the listed applicant for IL MCL-2 COAGULATION ANALYZER?
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 IL MCL-2 COAGULATION ANALYZER?
The FDA product code for IL MCL-2 COAGULATION ANALYZER is GKP.
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: GKP)
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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