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FDA 510(k)

N2 TEST

K-Number: K843840 · 1984-10-12

ApplicantErich Jaeger, Inc.
Decision Date1984-10-12
Product Code
DecisionSubstantially Equivalent

Device Summary

N2 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 K843840. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N2 TEST?

N2 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 K843840.

When did N2 TEST receive FDA 510(k) clearance?

N2 TEST received FDA 510(k) clearance on 1984-10-12, under 510(k) number K843840.

Who is the listed applicant for N2 TEST?

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

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.

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