FDA applicant
Precitron A.B.
FDA records 1 decision for Precitron A.B. (Uppsala, SE) in 1999: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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 Precitron A.B.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Precitron A.B. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Precitron A.B.’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