FDA applicant

Ellis Pharmaceutical Consulting, Inc.

Princeton, NJ5 decisions1983–19910 recalls

FDA records 5 decisions for Ellis Pharmaceutical Consulting, Inc. (Princeton, NJ) from 1983 to 1991: 5 510(k) clearances. Most are in product codes JAQ (System, Applicator, Radionuclide…) and KPE (Container, I.V.). 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 Ellis Pharmaceutical Consulting, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ellis Pharmaceutical Consulting, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ellis Pharmaceutical Consulting, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?