Windy Hill Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DUCPREP BREAST ASPIRATOR, MODEL PMPO2, FUJI CATHETER, MODEL CTH001
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Windy Hill Technology, Inc. Gastroenterology & Urology ✕
2 devices