# Rossmax International, Ltd.

- Location (FDA's records): Taipei, TW
- FDA decisions: 16 (1998–2006): 16 510(k) clearances
- Product codes: DXN (14), DPW (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Fego Precision Industrial Co;, Ltd.: 1 (https://510kreport.com/company/fego-precision-industrial)
- Gocanning Technology, Ltd.: 1 (https://510kreport.com/company/gocanning-technology)

## Its most-cited devices
- K021225: Rossmax Automatic Blood Pressure Monitor, Model Cardiocare 1000I (2002), cited by 2

## Recent decisions
- K060342: Rossmax Automatic Blood Pressure Monitor Model MO701K (Apr 4, 2006)
- K052727: Rossmax Non-Invasive Blood Pressure Monitors, Models S380, K350 (Dec 16, 2005)
- K021225: Rossmax Automatic Blood Pressure Monitor, Model Cardiocare 1000I (May 22, 2002)
- K013539: Rossmax Medipro, Models 100F, 200F, and 300F Blood Pressure Monitors (Jan 17, 2002)
- K013583: Rossmax Medipro Model 10 and 60, Medicare Model 10 and 60 Blood Pressure Monitors (Jan 17, 2002)
- K011539: Rossmax Medipro Model 100, Model 200, and Model 300 Blood Pressure Monitors (Jul 20, 2001)
- K011352: Rossmax Smartinflate Cardiopro, Model 1000I and Model 3000I Blood Pressure Monitors (Jul 20, 2001)
- K011523: Rossmax Automatic Wristwatch Blood Pressure Monitor, Model BPW138 (Jun 14, 2001)

Source page: https://510kreport.com/company/rossmax-international