# Acotec Scientific Co., Ltd.

- Location (FDA's records): Beijing, CN
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Covidien: 2 (https://510kreport.com/company/covidien)

## Recent decisions
- K250688: Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™ Endovenous Radiofrequency Catheter (ERA-C30-US); Endovenous Radiofrequency Generator (ERA-G5-US) (Oct 7, 2025)

Source page: https://510kreport.com/company/acotec-scientific