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FDA 510(k)

IL TEST PROS

K-Number: K011424 · 2001-06-25

Decision Date2001-06-25
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IL TEST PROS 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 2001-06-25 under 510(k) number K011424. 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 PROS?

IL TEST PROS is a medical device that received FDA 510(k) clearance on 2001-06-25. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K011424.

When did IL TEST PROS receive FDA 510(k) clearance?

IL TEST PROS received FDA 510(k) clearance on 2001-06-25, under 510(k) number K011424.

Who is the listed applicant for IL TEST PROS?

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 PROS?

The FDA product code for IL TEST PROS is GGP.

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.

View all 315 devices →

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

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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