# Midmark Diagnostics Group

- Location (FDA's records): Torrance, CA
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: MWI (1)
- Predicates its devices cite: 3 (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
- Cas Medical Systems, Inc.: 1 (https://510kreport.com/company/cas-medical-systems)
- Welch Allyn, Inc.: 1 (https://510kreport.com/company/welch-allyn)
- Y: 1 (https://510kreport.com/company/y)

## Firms that cite its devices most
- Midmark Corp.: 1 (https://510kreport.com/company/midmark)

## Its most-cited devices
- K072516: Midmark Diagnostics Iqmark Vital Signs Monitor (2007), cited by 1

## Recent decisions
- K072516: Midmark Diagnostics Iqmark Vital Signs Monitor (Oct 18, 2007)

Source page: https://510kreport.com/company/midmark-diagnostics-group