510(k) Report

FDA applicant

Autogenic Systems

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Autogenic Systems (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code JJG (Analyzer, Chemistry, Centrifugal, For Clinical…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Autogenic Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Autogenic Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Autogenic Systems by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Autogenic Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • JJGAnalyzer, Chemistry, Centrifugal, For Clinical Use1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K781900Analyzer, Automed CentrifugalAutogenic Systems · 19781cites it

What has FDA decided for it lately?

  • K781900Analyzer, Automed CentrifugalAutogenic Systems · 1978

The one decision as Autogenic Systems →