# Mobilemedtek

- Location (FDA's records): Louisville, KY
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: GWQ (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: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mitsar Co., Ltd.: 1 (https://510kreport.com/company/mitsar)
- Carefusion 209, Inc.: 1 (https://510kreport.com/company/carefusion-209)
- Nihon Kohden America, Inc.: 1 (https://510kreport.com/company/nihon-kohden-america)

## Firms that cite its devices most
- Seer Medical Pty, Ltd.: 1 (https://510kreport.com/company/seer-medical)

## Its most-cited devices
- K170441: ElectroTek (2017), cited by 1

## Recent decisions
- K170441: ElectroTek (Jun 5, 2017)

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