FDA applicant
Midwest Metabolic Support Group
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
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.
Planning a device like Midwest Metabolic Support Group’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Midwest”
FDA records each applicant name separately; these may or may not be the same firm.