FDA applicant
Zimmar Consulting, Ltd.
FDA records 17 decisions for Zimmar Consulting, Ltd. (Mchenry, IL) from 1984 to 1986: 17 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and FMF (Syringe, Piston). 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 Zimmar Consulting, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Zimmar Consulting, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Zimmar Consulting, Ltd.’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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