FDA applicant

Immuno Nuclear Corp.

Stillwater, MN30 decisions1981–19860 recalls

FDA records 30 decisions for Immuno Nuclear Corp. (Stillwater, MN) from 1981 to 1986: 30 510(k) clearances. Most are in product codes DHB (System, Test, Radioallergosorbent (Rast)…) and CEW (Radioimmunoassay, Parathyroid Hormone). 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 Immuno Nuclear Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Immuno Nuclear Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Immuno Nuclear 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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Other applicant names beginning “Immuno”

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

Immuno Concepts, Inc. 36 Immuno-Mycologics, Inc. 26 Immuno-Products Industries 12 Immuno Assay Corp. 10 Immuno-Diagnostic Products, Inc. 8 Immuno Concepts, N.A., Ltd. 4 Immuno Diagnostic Center, Inc. 3 Immuno-Diagnostic Laboratories 2 Immuno-U.S., Inc. 1 Immuno Pathology Labs 1

Immuno Nuclear Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Immuno”