# Kli

- Location (FDA's records): Mchenry, IL
- FDA decisions: 18 (1977–1980): 18 510(k) clearances
- Product codes: HET (9), KNF (3), HIN (2), HIF (2), FGC (1), FAP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K800822: CO2 Cystoscopy/Urethroscopy Console (Jun 17, 1980)
- K800913: Gynecological Cysto/Urethroscope (May 14, 1980)
- K781913: Insuffalator Laparaoscopic (Dec 4, 1978)
- K781109: Forceps, Electrosurgical (Sep 14, 1978)
- K781089: One Incision BI-Polar Electro. Forceps (Jul 17, 1978)
- K780954: Scissors, Hook, Electrosurgical (Jun 22, 1978)
- K780955: Scissors, Hook, Electrosurgical (Jun 22, 1978)
- K772297: Insufflator, Model G100 & 200 (Jan 5, 1978)

Source page: https://510kreport.com/company/kli