FDA applicant
Jamieson Film Co.
FDA records 6 decisions for Jamieson Film Co. (Dallas, TX) from 1991 to 1997: 6 510(k) clearances. Most are in product codes IZI (System, X-Ray, Angiographic) and IXX (Processor, Cine Film). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Jamieson Film Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Jamieson Film Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Jamieson Film 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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