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FDA 510(k)

IL TEST IGG IGA & IGM KITS

K-Number: K833841 · 1984-01-04

ApplicantInstrumentation Laboratory CO
Decision Date1984-01-04
Product CodeCZK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

IL TEST IGG IGA & IGM KITS 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 1984-01-04 under 510(k) number K833841. The device is classified under product code CZK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL TEST IGG IGA & IGM KITS?

IL TEST IGG IGA & IGM KITS is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K833841.

When did IL TEST IGG IGA & IGM KITS receive FDA 510(k) clearance?

IL TEST IGG IGA & IGM KITS received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833841.

Who is the listed applicant for IL TEST IGG IGA & IGM KITS?

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 IGG IGA & IGM KITS?

The FDA product code for IL TEST IGG IGA & IGM KITS is CZK.

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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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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