FDA applicant
Oakfield Instruments, Ltd.
FDA records 8 decisions for Oakfield Instruments, Ltd. (Oxon Ox8 1ja England, GB) from 1989 to 1997: 8 510(k) clearances. Most are in product codes KLA (Monitor, Esophageal Motility, Anorectal…) and IZD (Probe, Uptake, Nuclear). 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 Oakfield Instruments, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Oakfield Instruments, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Oakfield Instruments, 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