Ad-Tech Medical Instrument Corp - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Ad-Tech Medical Instrument Corp has 17 FDA 510(k) cleared neurology devices. Based in Racine, US.
Historical record: 17 cleared submissions from 1985 to 2012.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
18 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
Sep 19, 1995
AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGS
Anesthesiology
603d
Cleared
Jan 20, 1995
CUEVA CRANIAL NERVE ELECTRODE
Neurology
154d
Cleared
Nov 23, 1992
AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC
Neurology
88d