FDA applicant
Kilang Barangan Getah Dioh
FDA records 2 decisions for Kilang Barangan Getah Dioh (Negeri Sembilan, MY) in 1999: 2 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 Kilang Barangan Getah Dioh’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kilang Barangan Getah Dioh since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kilang Barangan Getah Dioh’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