IL TEST PROS
K-Number: K011424 · 2001-06-25
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Device Summary
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.
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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