Medical Device Manufacturer · US , Temecula , CA

Guidcorp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Guidcorp Cardiovascular ✕

1 devices

1-1 of 1

Cleared May 14, 2003

HI-TORQUE PILOT 50 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE...

Cardiovascular · 82d