FDA applicant
Vicon Instrument Co.
FDA records 8 decisions for Vicon Instrument Co. (Mchenry, IL) from 1976 to 1981: 8 510(k) clearances. Most are in product codes ESD (Hearing Aid, Air-Conduction, Prescription) and KLW (Masker, Tinnitus). 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 Vicon Instrument Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Vicon Instrument Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Vicon Instrument Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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