FDA applicant
Richard Scott Elliott
FDA records 1 decision for Richard Scott Elliott (Salem, OR) in 1985: 1 510(k) clearance. All are in product code LOJ (Kit, Test,Alpha-Fetoprotein For Testicular…). 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 Richard Scott Elliott’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Richard Scott Elliott since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Richard Scott Elliott’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 “Richard”
FDA records each applicant name separately; these may or may not be the same firm.