FDA applicant
Cottrell, Ltd.
FDA records 9 decisions for Cottrell, Ltd. (North Attleboro, MA) from 1990 to 1999: 9 510(k) clearances. Most are in product codes MED (Sterilant, Medical Devices) and LRJ (Disinfectant, Medical Devices). Its devices cite 5 predicates, 1 of them its own earlier devices. 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 Cottrell, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cottrell, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cottrell, Ltd.’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) Report