# Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 2 (2019–2024): 2 510(k) clearances
- Product codes: DTE (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K182839: Lifetech Cardio Model 8301 Temporary Pacemaker (2019), cited by 1

## Recent decisions
- K232721: Lifetech Cardio Temporary Pacemaker (Jan 7, 2024)
- K182839: Lifetech Cardio Model 8301 Temporary Pacemaker (Feb 28, 2019)

Source page: https://510kreport.com/company/shenzhen-lifetech-cardio-medical-electronics