Navion Biomedical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Navion Biomedical Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Navion Biomedical Corp. has 5 FDA 510(k) cleared medical devices. Based in Holbrook, US.
Historical record: 5 cleared submissions from 1990 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Navion Biomedical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Navion Biomedical Corp.
5 devices
Cleared
Mar 01, 1999
BIONAVIGATION SYSTEM FOR PLACEMENT OF ENTERAL FEEDING TUBES
Gastroenterology & Urology
150d
Cleared
Nov 12, 1997
1.4 FR MAPCATH SENSOR STYLET
General Hospital
89d
Cleared
Aug 25, 1995
MAPWIRE J-TIP SENSOR GUIDEWIRE
General Hospital
78d
Cleared
Jun 02, 1994
NAVIGATOR-MP CATHETER LOCATION INSTRUMENT
General Hospital
127d
Cleared
Aug 22, 1990
NAVION SMART-WIRE(TM) CATHETER LOCATION SYSTEM
General Hospital
159d