# Kells Medical, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1982–1993): 12 510(k) clearances
- Product codes: KPE (2), LIX (1), NAD (1), KCJ (1), BXP (1), KNT (1), KGX (1), ESE (1), ETY (1), ETF (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
- K926333: CPR Plus (Nov 8, 1993)
- K890093: PVC Empty Solution Container Enteral Pump Set (Jul 24, 1989)
- K890095: PVC Empty Solution Container W/3 Lead Transfer Set (May 24, 1989)
- K890094: Eva Empty Solution Container W/3 Lead Transfer Set (May 24, 1989)
- K861972: Dermistrip (Jun 27, 1986)
- K844463: Dermidress (Jan 8, 1985)
- K844072: Dermizip Skin Closure Device (Nov 5, 1984)
- K832678: Phonatory Function Analyzer PS-77 (Mar 7, 1984)

Source page: https://510kreport.com/company/kells-medical