Neurocom International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurocom International, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Neurocom International, Inc. has 5 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 5 cleared submissions from 1985 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Neurocom International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurocom International, Inc.
5 devices
Cleared
Aug 04, 1995
BALANCE MANAGER
Physical Medicine
225d
Cleared
Sep 10, 1991
EMG ACCESSORY FOR POSTUROGRAPHY
Neurology
511d
Cleared
Jul 16, 1987
NEUROCOM PRESSURE TEST SYSTEM
Ear, Nose, Throat
79d
Cleared
Sep 17, 1986
DUAL FORCEPLATE
Physical Medicine
12d
Cleared
Aug 05, 1985
EQUITEST
Ear, Nose, Throat
98d