Guidcorp is one of 25821 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Guidcorp - FDA 510(k) Cleared Devices
Recent clearances: HI-TORQUE PILOT 50 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE PILOT 150 GUIDE WIRE WITH HYDROCOAT HYDROPHG
1
Total
1
Cleared
0
Denied
Guidcorp has 1 FDA 510(k) cleared medical devices. Based in Temecula, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Guidcorp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Guidcorp
1 devices