# Kelleher Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 94 (1982–1983): 94 510(k) clearances
- Product codes: EQN (6), KTG (5), EQH (4), GBB (3), GWN (2), EOQ (2), EPT (2), FSO (2), ETF (2), KAD (2), KAI (2), JEK (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K822618: Emergency Tracheostomy Instrument Set (Jan 28, 1983)
- K822268: Nagashima NS-Iii Electronystagmograph (Jan 28, 1983)
- K823083: Electrosurgical Unit (Dec 7, 1982)
- K823111: Nystymograph Access (Nov 22, 1982)
- K822252: Ent Treatment Units (Nov 22, 1982)
- K822272: Head Mirrors W/Head Lamps & Head Bands (Nov 10, 1982)
- K822017: Tympanostomy Tubes & Various Types (Oct 27, 1982)
- K822257: Various Types of Light Source Handles (Oct 26, 1982)

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