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FDA 510(k)

ALVEO-DIFFUSION TEST

K-Number: K853443 · 1986-02-21

ApplicantErich Jaeger, Inc.
Decision Date1986-02-21
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ALVEO-DIFFUSION 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 1986-02-21 under 510(k) number K853443. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALVEO-DIFFUSION TEST?

ALVEO-DIFFUSION TEST is a medical device that received FDA 510(k) clearance on 1986-02-21. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K853443.

When did ALVEO-DIFFUSION TEST receive FDA 510(k) clearance?

ALVEO-DIFFUSION TEST received FDA 510(k) clearance on 1986-02-21, under 510(k) number K853443.

Who is the listed applicant for ALVEO-DIFFUSION 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 ALVEO-DIFFUSION TEST?

The FDA product code for ALVEO-DIFFUSION TEST is BZC.

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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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