FDA 510(k)

CO TEST

K-Number: K843845 · 1984-10-12

Decision Date1984-10-12

Product CodeCCJ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CO TEST is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger, Inc.. It received FDA 510(k) clearance on 1984-10-12 under 510(k) number K843845. The device is classified under product code CCJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO TEST?

CO TEST is a medical device that received FDA 510(k) clearance on 1984-10-12. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K843845.

When did CO TEST receive FDA 510(k) clearance?

CO TEST received FDA 510(k) clearance on 1984-10-12, under 510(k) number K843845.

Who is the listed applicant for CO TEST?

The FDA 510(k) record lists Erich Jaeger, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CO TEST?

The FDA product code for CO TEST is CCJ.

Other records listing Erich Jaeger, Inc. 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.