FDA applicant

Norwich Eaton Pharmaceuticals, Inc.

Mchenry, IL10 decisions1980–19840 recalls

FDA records 10 decisions for Norwich Eaton Pharmaceuticals, Inc. (Mchenry, IL) from 1980 to 1984: 10 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and KHT (Fraction V, Antigen, Antiserum, Control). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Norwich Eaton Pharmaceuticals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Norwich Eaton Pharmaceuticals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Norwich”

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

Norwich Pharmacal Co. 1

Norwich Eaton Pharmaceuticals, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Norwich”