Medical Device Manufacturer · US , Kirkland , WA

Vadiswire Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Recent clearances: ZIGIWIRE MODE2 GUIDEWIRE WIRE SYSTEM, ZIGIWIRE MODE3 GUIDEWIRE WIRE SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vadiswire Corporation Cardiovascular ✕

1 devices

1-1 of 1

Cleared Dec 18, 2014

ZIGIWIRE MODE2 GUIDEWIRE WIRE SYSTEM, ZIGIWIRE MODE3 GUIDEWIRE WIRE SYSTEM

Cardiovascular · 220d