FDA applicant
Hamilton Co.
FDA records 16 decisions for Hamilton Co. (Mchenry, IL) from 1980 to 1996: 16 510(k) clearances. Most are in product codes JQW (Station, Pipetting And Diluting, For Clinical…) and JTC (Device, Microtiter Diluting/Dispensing). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Hamilton Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hamilton Co. since 2007.
Recalls per year
1in 2011
Class I Class II/III not classified
Planning a device like Hamilton Co.’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 “Hamilton”
FDA records each applicant name separately; these may or may not be the same firm.