Neuro Technology - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Neuro Technology has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1982 to 1993. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Neuro Technology Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 19, 1993
E-SP COMBINED EPI SPINAL MINISET
Anesthesiology
199d
Cleared
May 30, 1991
MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE
Anesthesiology
405d
Cleared
May 28, 1991
ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLE
Anesthesiology
403d
Cleared
Sep 13, 1982
STIMPEN
Anesthesiology
56d
Cleared
Jul 30, 1982
NEUROSTIM II
Anesthesiology
11d