FDA applicant

Pheragen Technology Corp.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Pheragen Technology Corp. (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code GKT (Separator, Automated, Blood Cell, Diagnostic). 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, hematology panel, where it files most

How often FDA has decided Pheragen Technology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pheragen Technology Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pheragen Technology 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

Pheragen Technology Corp.

Which product codes does it file in?

What has FDA decided for it lately?