Excelsior Medical Corporation is one of 20342 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Excelsior Medical Corporation - FDA 510(k) Cleared Devices
Recent clearances: 0.9% Sodium Chloride Injection, USP - 2.5 mL in 3 mL Syringe, 0.9% Sodium Chloride Injection, USP-3mL in 10 mL Syringe, 0.9% Sodium Chloride Injection, USP - 5 mL in 10 mL Syringe, 0.9% Sodium Chloride Injection, USP - 10 mL in 10 mL Syringe, HEPARIN LOCK / FLUSH SYRINGES
2
Total
2
Cleared
0
Denied
Excelsior Medical Corporation has 2 FDA 510(k) cleared medical devices. Based in Neptune, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Excelsior Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Excelsior Medical Corporation
2 devices