510(k) Report

FDA applicant

Radcal Corp.

Mchenry, IL4 decisions1982–19840 recalls

FDA records 4 decisions for Radcal Corp. (Mchenry, IL) from 1982 to 1984: 4 510(k) clearances. All are in product code KPT (Calibrator, Dose, Radionuclide). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Radcal Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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