Ad-Tech Medical Instrument Corp - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ad-Tech Medical Instrument Corp Neurology ✕
16 devices
Cleared
Apr 24, 2012
BRAIN BIOPSY NEEDLE
Neurology
277d
Cleared
May 30, 2006
DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES,...
Neurology
179d
Cleared
May 25, 2006
DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH...
Neurology
174d
Cleared
Aug 16, 2004
MACRO-MICRO DEPTH ELECTRODE
Neurology
63d
Cleared
Nov 02, 1999
AD-TECH'S FORAMEN OVALE ELECTRODE
Neurology
237d
Cleared
Sep 13, 1999
CORTICAL MAPPING UNIT, MODEL CMU
Neurology
76d
Cleared
Jun 10, 1998
AD-TECH'S SPINAL ELECTRODE
Neurology
272d
Cleared
May 09, 1997
AD-TECH'S DEPTH ELECTRODE
Neurology
190d
Cleared
May 09, 1997
AD-TECH SUBDURAL ELECTRODE
Neurology
80d
Cleared
Jan 20, 1995
CUEVA CRANIAL NERVE ELECTRODE
Neurology
154d
Cleared
Nov 23, 1992
AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC
Neurology
88d
Cleared
Oct 23, 1992
AD-TECH SUB DURAL ELECTRODEDS
Neurology
86d
Cleared
Jan 15, 1992
AD-TECH EPIDURAL PEG ELECTRODE
Neurology
205d
Cleared
Jul 27, 1989
AD-TECH'S DEPTH ELECTRODE
Neurology
122d
Cleared
Aug 25, 1986
WYLER SPHENOIDAL ELECTRODE
Neurology
160d
Cleared
Jul 30, 1985
WYLER SUBDURAL STRIP ELECTRODE
Neurology
183d