510(k) Report

FDA applicant

Nova Corp.

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Nova Corp. (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code CGZ (Electrode, Ion-Specific, Chloride). 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 Nova Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nova Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nova Corp.’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?

  • CGZElectrode, Ion-Specific, Chloride1decision

What has FDA decided for it lately?

  • K790653Nova 3 Chloride/Total Dioxide AnalyzerNova Corp. · 1979

The one decision as Nova Corp. →

Other applicant names beginning “Nova”

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

Nova Biomedical Corp. 129Nova-Ventrx 12Nova Medical Specialties 11Nova Technology Corp. 3Nova Health Systems, Inc. 3Nova Medical, Inc. 1Nova Technologies, Inc. 1Nova/Da Vinci Systems, Inc. 1Nova Design Technologies, Ltd. 1Nova Therapeutic System 1Nova Ranger, Inc. 1Nova Rubber Glove Industries Sdn. Bhd. 1