App Pharmaceuticals, LLC is one of 24655 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
App Pharmaceuticals, LLC - FDA 510(k) Cleared Devices
Recent clearances: HEPARIN LOCK FLUSH SOLUTION USP, MODELS 504401, 504411, 504505, 505701, 504901, 1710
1
Total
1
Cleared
0
Denied
App Pharmaceuticals, LLC has 1 FDA 510(k) cleared medical devices. Based in Appollo Beach, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by App Pharmaceuticals, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - App Pharmaceuticals, LLC
1 devices