Viratek, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Viratek, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 4 cleared submissions from 1985 to 1990. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Viratek, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 09, 1990
SPAG PAK
Anesthesiology
139d
Cleared
Aug 01, 1988
AEROSOL DELIVERY HOOD
Anesthesiology
52d
Cleared
Oct 06, 1987
SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE
Anesthesiology
273d
Cleared
Oct 06, 1987
(SPAG) MODEL SPAG-2 6000 SERIES
Anesthesiology
180d
Cleared
Dec 30, 1985
VIRATEK SMALL PARTICLE AEROSOL GENERAT
Cardiovascular
465d