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FDA 510(k)

IL 501, NA/K ANALYZER

K-Number: K812762 · 1981-10-20

ApplicantInstrumentation Laboratory CO
Decision Date1981-10-20
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IL 501, NA/K ANALYZER 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 1981-10-20 under 510(k) number K812762. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL 501, NA/K ANALYZER?

IL 501, NA/K ANALYZER is a medical device that received FDA 510(k) clearance on 1981-10-20. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K812762.

When did IL 501, NA/K ANALYZER receive FDA 510(k) clearance?

IL 501, NA/K ANALYZER received FDA 510(k) clearance on 1981-10-20, under 510(k) number K812762.

Who is the listed applicant for IL 501, NA/K 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 501, NA/K ANALYZER?

The FDA product code for IL 501, NA/K ANALYZER is JGS.

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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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