# Oximetrix, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1976–1986): 12 510(k) clearances
- Product codes: DQE (3), GEI (2), DYG (2), DQA (1), JSJ (1), DXG (1), DRY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Hospira, Inc.: 4 (https://510kreport.com/company/hospira)
- Abbott Laboratories: 1 (https://510kreport.com/company/abbott-laboratories)

## Its most-cited devices
- K820674: Opticath (1982), cited by 2
- K821057: Flow Directed Thermal-Dilution Infusion (1982), cited by 1
- K853018: Model 3000 Opticath Computer (1986), cited by 1
- K823007: Opticath Heparin Coated, Flow-Direct (1982), cited by 1

## Recent decisions
- K853018: Model 3000 Opticath Computer (Jan 13, 1986)
- K842622: Hemo Static/Esu Scalpel System (Oct 23, 1984)
- K833966: Pump Infusion Wearable Infusion Pump (Jan 25, 1984)
- K823007: Opticath Heparin Coated, Flow-Direct (Nov 1, 1982)
- K821056: Flow Directed Thermal-Dilution Catheter (May 18, 1982)
- K821057: Flow Directed Thermal-Dilution Infusion (May 18, 1982)
- K820674: Opticath (Mar 25, 1982)
- K811391: Oximetrix Accu Sat CPB (Jul 20, 1981)

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