Luxtron is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Luxtron - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Luxtron has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1982 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Luxtron Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luxtron
4 devices
Cleared
Mar 28, 1994
LUXTRON MODEL 3100/3101/3102 MULTICHANNEL
General Hospital
636d
Cleared
Aug 19, 1986
MODEL 3000 MLULTICHANNEL FLUOROPTIC THERMOMETER
General Hospital
112d
Cleared
Jul 03, 1984
MULTICHANNEL 2000 FLUOROPTIC THERMOMET
General Hospital
111d
Cleared
Jul 13, 1982
BIOMEDICAL FLUOROPTIC
General Hospital
88d