# Dk Medical Technology Co., Ltd.

- Location (FDA's records): Suzhou, CN
- FDA decisions: 3 (2023–2025): 3 510(k) clearances
- Product codes: PNO (2), LIT (1)
- Predicates its devices cite: 3 (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
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Recent decisions
- K242254: D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter (Apr 21, 2025)
- K232207: D·Kutting™ PTA Scoring Balloon Dilatation Catheter (Mar 7, 2024)
- K214009: D·Kaptain PTA High Pressure Balloon Dilatation Catheter (Apr 5, 2023)

Source page: https://510kreport.com/company/dk-medical-technology