FDA applicant
National-Standard Medical Products
FDA records 3 decisions for National-Standard Medical Products (Gainesville, FL) in 1990: 3 510(k) clearances. Most are in product codes GAA (Needle, Aspiration And Injection, Disposable) and DOX (Fluorometer, Lead (Dedicated Instruments)). 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 National-Standard Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for National-Standard Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like National-Standard Medical Products’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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