FDA applicant
Med-Pak Corp.
FDA records 2 decisions for Med-Pak Corp. (Canada H4r 2k3, CA) from 1981 to 1989: 2 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and FKG (Tray, Start/Stop (Including Contents), Dialysis). 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 Med-Pak Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Med-Pak Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Med-Pak Corp.’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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