Sascie is one of 7050 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sascie - FDA 510(k) Cleared Devices
Recent clearances: SAS SERUM/URINE HCG, SAS PREGNANCY STRIP
2
Total
2
Cleared
0
Denied
Sascie has 2 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Sascie Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sascie
2 devices