Rocap Div. of Sabratek Corp. is one of 7927 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rocap Div. of Sabratek Corp. - FDA 510(k) Cleared Devices
Recent clearances: ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML, HEPARIN IV FLUSH SYRINGE, 10 U/ML \, NORMAL SALINE FLUSH SYRINGE
3
Total
3
Cleared
0
Denied
Rocap Div. of Sabratek Corp. has 3 FDA 510(k) cleared medical devices. Based in Orlando, US.
Historical record: 3 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rocap Div. of Sabratek Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rocap Div. of Sabratek Corp.
3 devices