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FDA 510(k)

IL TEST FREE PROTEIN S

K-Number: K010379 · 2001-04-13

Decision Date2001-04-13
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL TEST FREE PROTEIN S 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 2001-04-13 under 510(k) number K010379. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL TEST FREE PROTEIN S?

IL TEST FREE PROTEIN S is a medical device that received FDA 510(k) clearance on 2001-04-13. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K010379.

When did IL TEST FREE PROTEIN S receive FDA 510(k) clearance?

IL TEST FREE PROTEIN S received FDA 510(k) clearance on 2001-04-13, under 510(k) number K010379.

Who is the listed applicant for IL TEST FREE PROTEIN S?

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 TEST FREE PROTEIN S?

The FDA product code for IL TEST FREE PROTEIN S is GGP.

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: GGP)

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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