Cns, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Cns, Inc. has 14 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 14 cleared submissions from 1984 to 1996. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cns, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
May 30, 1996
BREATHE RIGHT NASAL STRIP
Ear, Nose, Throat
164d
Cleared
Feb 27, 1996
BREATHE RIGHT NASAL STRIP
Ear, Nose, Throat
124d
Cleared
Oct 20, 1995
BREATHE RIGHT NASAL STRIP
Ear, Nose, Throat
67d
Cleared
Sep 19, 1995
SLEEP TEST(TM)
Anesthesiology
239d
Cleared
Oct 07, 1993
BREATHE RIGHT
Ear, Nose, Throat
573d
Cleared
Oct 18, 1991
AM-PAK
Neurology
137d
Cleared
Jul 10, 1991
SLEEP I/T-5 AND SLEEP I/T-8
Anesthesiology
285d
Cleared
Apr 16, 1991
RESPI-PAK RT-PAK
Anesthesiology
74d
Cleared
Oct 24, 1990
CNS SATELLITE 100, 200, 1000, 2000 ELECTROENCE.
Neurology
204d
Cleared
Mar 12, 1990
POLY G PHYSIOLOGICAL DATA RECORDER
Anesthesiology
81d
Cleared
May 29, 1986
CNS 4/8 AND CT 48.1 SOFTWARE
Neurology
85d
Cleared
Apr 17, 1986
CNS-EP SYSTEM AND EP 1.0 SOFTWARE
Neurology
84d
Cleared
Jan 10, 1986
CNS-16 & LTM 1.0 SOFTWARE
Neurology
91d
Cleared
Dec 17, 1984
CEREBRAL TRACER 1500 & CT 1.0 SOFTWARE
Neurology
66d