FDA applicant

Ackerman Nuclear, Inc.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Ackerman Nuclear, Inc. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code DPA (Apparatus, General Use, Thin Layer…). 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 Ackerman Nuclear, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ackerman Nuclear, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ackerman Nuclear, Inc.’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 “Ackerman”

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

Ackerman-Schmehl Industries, Inc. 1

Ackerman Nuclear, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ackerman”