Novacon Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novacon Corp. - FDA 510(k) Cleared Devices
6
Total
4
Cleared
0
Denied
Novacon Corp. has 4 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 4 cleared submissions from 1994 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Novacon Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Novacon Corp.
6 devices
Cleared
Sep 10, 1999
FREEDOM INFUSION SYSTEM
General Hospital
87d
Cleared
Aug 05, 1996
DIB INFUSOR
General Hospital
222d
Cleared
Aug 05, 1996
DIB INFUSOR-RA
General Hospital
195d
Cleared
Feb 14, 1995
DIB INFUSORS
General Hospital
155d
Cleared
Aug 05, 1994
DIB INFUSOR
General Hospital
116d
Cleared
Feb 25, 1994
DIB INFUSOR
General Hospital
395d