Schiff & Co. - FDA 510(k) Cleared Devices
Recent clearances: X-TIP INTRAOSSEOUS PERFORATOR, JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200, NUTRISAFE ENTERAL FEEDING TUBE
15
Total
15
Cleared
0
Denied
FDA 510(k) Regulatory Record - Schiff & Co. Cardiovascular ✕
1 devices