Nephron Pharmaceuticals Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nephron Pharmaceuticals Corporation - FDA 510(k) Cleared Devices
Recent clearances: Nephron Nitrile Powder-Free Nitrile Examination Gloves (Tested For Use With Chemotherapy Drugs)
1
Total
1
Cleared
0
Denied
Nephron Pharmaceuticals Corporation has 1 FDA 510(k) cleared medical devices. Based in West Columbia, US.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nephron Pharmaceuticals Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Nephron Pharmaceuticals Corporation
1 devices