# Chest M.I., Inc.

- Location (FDA's records): Austin, TX
- FDA decisions: 2 (2009–2009): 2 510(k) clearances
- Product codes: BZG (2)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Puritan Bennett Corp.: 1 (https://510kreport.com/company/puritan-bennett)
- Micro Direct, Inc.: 1 (https://510kreport.com/company/micro-direct)
- Iqteq Development: 1 (https://510kreport.com/company/iqteq-development)
- Brentwood Medical Technology Corp.: 1 (https://510kreport.com/company/brentwood-medical-technology)

## Firms that cite its devices most
- Mehow Innovative, Ltd.: 1 (https://510kreport.com/company/mehow-innovative)

## Its most-cited devices
- K090646: Cardiotech Spirometry System, Model GT-105 (2009), cited by 1

## Recent decisions
- K090646: Cardiotech Spirometry System, Model GT-105 (Jul 23, 2009)
- K080921: Spiro-Master PC-10 Spirometry System (Jan 21, 2009)

Source page: https://510kreport.com/company/chest-mi