FDA applicant

Electrophoresis Corp. of America

Mchenry, IL27 decisions1978–19800 recalls

FDA records 27 decisions for Electrophoresis Corp. of America (Mchenry, IL) from 1978 to 1980: 27 510(k) clearances. Most are in product codes CEF (Electrophoretic, Protein Fractionation) and JJN (Apparatus, Electrophoresis, For Clinical Use). 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 Electrophoresis Corp. of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electrophoresis Corp. of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Electrophoresis”

FDA records each applicant name separately; these may or may not be the same firm.

Electrophoresis Corp. 4

Electrophoresis Corp. of America

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Electrophoresis”