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FDA 510(k)

IL T UPTAKE ASSAY SYSTEM

K-Number: K903396 · 1990-10-12

Decision Date1990-10-12
Product CodeKHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL T UPTAKE ASSAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K903396. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL T UPTAKE ASSAY SYSTEM?

IL T UPTAKE ASSAY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K903396.

When did IL T UPTAKE ASSAY SYSTEM receive FDA 510(k) clearance?

IL T UPTAKE ASSAY SYSTEM received FDA 510(k) clearance on 1990-10-12, under 510(k) number K903396.

Who is the listed applicant for IL T UPTAKE ASSAY SYSTEM?

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 T UPTAKE ASSAY SYSTEM?

The FDA product code for IL T UPTAKE ASSAY SYSTEM is KHQ.

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.

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Related Devices (Code: KHQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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