FDA applicant
Frederic J. Toye, M.D.
FDA records 6 decisions for Frederic J. Toye, M.D. (Walker, MI) from 1980 to 1987: 6 510(k) clearances. All are in product code BTO (Tube, Tracheostomy (W/Wo Connector)). 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 Frederic J. Toye, M.D.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Frederic J. Toye, M.D. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Frederic J. Toye, M.D.’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