# Neich Medical (Shenzhen) Company Limited

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2002–2004): 3 510(k) clearances
- Names in FDA's records: Neich Medical (Shenzhen) Company Limited (2); Neich Medical(Shenzhen)Company, Ltd. (1)
- Product codes: DQY (1), DYB (1), DQO (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
- K032888: Creation NM Diagnostic Catheters (Feb 24, 2004)
- K030715: Saffron NM Guiding Catheter (Apr 24, 2003)
- K020964: Neich NM Advance Catheter Sheath Introducer (Oct 11, 2002)

Source page: https://510kreport.com/company/neich-medical-shenzhen
