FDA applicant
Kli
FDA records 18 decisions for Kli (Mchenry, IL) from 1977 to 1980: 18 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and KNF (Coagulator-Cutter, Endoscopic, Unipolar (And…). 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 Kli’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kli since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kli’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