Nephron Pharmaceuticals Corp. is one of 18369 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nephron Pharmaceuticals Corp. - FDA 510(k) Cleared Devices
Recent clearances: SODIUM CHLORDE INHALATION SOLUTION, 0.9% USP-3ML, SODIUM CHLORIDE INHALATION SOLUTION, 3%, 7%, AND 10%, USP-4ML
2
Total
2
Cleared
0
Denied
Nephron Pharmaceuticals Corp. has 2 FDA 510(k) cleared medical devices. Based in Orlando, US.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Nephron Pharmaceuticals Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nephron Pharmaceuticals Corp.
2 devices