# Shandong Qiaopai Group Co., Ltd.

- Location (FDA's records): Zibo, CN
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: FMI (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K073705: Model TW SB, Scalp Vein Set; Model TW LB, Sterile Hypodermic Needle (Mar 24, 2008)

Source page: https://510kreport.com/company/shandong-qiaopai-group