# Inspiron Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 20 (1976–1986): 20 510(k) clearances
- Product codes: CAF (4), BTT (3), BZO (1), CBC (1), CAI (1), BZA (1), KZD (1), BYJ (1), BXJ (1), BTM (1), CBO (1), BWF (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
- K860838: Inspiron Double Swivel Trach Adapter (Apr 9, 1986)
- K850346: Oxygen Concentrator (Feb 4, 1985)
- K843932: Vapor-Phase Humidifier Sys-Advanced (Oct 18, 1984)
- K840935: Manual Resuscitation System (Apr 5, 1984)
- K841158: Nebulo 28 Nebulizer Kit (Mar 30, 1984)
- K840418: Inspiratory/Expiratory Muscle Exercis (Feb 17, 1984)
- K834290: Inspiron Liquid Oxygen System (Feb 4, 1984)
- K772069: Vol. Ventilator Setup W/Out Nebulizer (Nov 15, 1977)

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