FDA applicant
Central Media
FDA records 14 decisions for Central Media (Sacramento, CA) in 1987: 14 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and KZI (Culture Media, Enriched). 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 Central Media’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Central Media since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Central Media’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