Medix Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medix Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1978 to 1994. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medix Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 01, 1994
EASIMIST ULTRASONIC NEBULIZER
Anesthesiology
745d
Cleared
Jul 24, 1992
MEDIX NEBULIZING SYSTEM CODE NO. 2000 AND 2001
Anesthesiology
312d
Cleared
Aug 29, 1985
MEDIX ELECTRONIC NEBULIZING SYSTEM
Anesthesiology
37d
Cleared
Oct 18, 1982
SYRINGE PUMP 209-100
General Hospital
63d
Cleared
Apr 19, 1978
NERVTRON-RX
Neurology
30d