FDA applicant
William E. Mckay
FDA records 1 decision for William E. Mckay (San Jose, CA) in 1993: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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 William E. Mckay’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for William E. Mckay since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like William E. Mckay’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 “William”
FDA records each applicant name separately; these may or may not be the same firm.