FDA applicant
Williams Medical Co.
FDA records 5 decisions for Williams Medical Co. (Anaheim, CA) from 1985 to 1989: 5 510(k) clearances. Most are in product codes KPE (Container, I.V.) and KPO (Dialysate Concentrate For Hemodialysis (Liquid…). 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 Williams Medical Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Williams Medical Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Williams Medical Co.’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) ReportOther applicant names beginning “Williams”
FDA records each applicant name separately; these may or may not be the same firm.