FDA applicant
Gil-Med Industries C/O Kegan & Kegan, Ltd.
FDA records 7 decisions for Gil-Med Industries C/O Kegan & Kegan, Ltd. (Chicago, IL) from 1984 to 1988: 7 510(k) clearances. Most are in product codes KPE (Container, I.V.) and KNT (Tubes, Gastrointestinal (And Accessories)). 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 Gil-Med Industries C/O Kegan & Kegan, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Gil-Med Industries C/O Kegan & Kegan, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Gil-Med Industries C/O Kegan & Kegan…’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