Medical Device Manufacturer · TW , Taipei

Rossmax International , Ltd. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1998

Recent clearances: ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K, ROSSMAX NON-INVASIVE BLOOD PRESSURE MONITORS, MODELS S380, K350, ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR, MODEL CARDIOCARE 1000I

16
Total
16
Cleared
0
Denied

Rossmax International , Ltd. has 16 FDA 510(k) cleared cardiovascular devices. Based in Taipei, TW.

Historical record: 16 cleared submissions from 1998 to 2006.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Center For Measurement Standards of Industrial as regulatory consultant.

FDA 510(k) Regulatory Record - Rossmax International , Ltd.

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