510(k) Report

FDA applicant

Midwest Metabolic Support Group

Mchenry, IL4 decisions1982–19850 recalls

FDA records 4 decisions for Midwest Metabolic Support Group (Mchenry, IL) from 1982 to 1985: 4 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and KOA (Surgical Instruments, G-U, Manual (And…). 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 Midwest Metabolic Support Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midwest Metabolic Support Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Midwest”

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