FDA applicant
Advocacy International, Ltd.
FDA records 13 decisions for Advocacy International, Ltd. (Washington, DC) from 1981 to 1988: 13 510(k) clearances. Most are in product codes KOC (Accessories, Blood Circuit, Hemodialysis) and CAK (Microfilter, Blood Transfusion). 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 Advocacy International, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Advocacy International, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advocacy International, Ltd.’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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