Excel Tech. , Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Excel Tech. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: XLTEK STIMULATOR PROBES, MODELS 105233, 105234, 105235, 105236, 105237 AND 105238, XLTEK CLEAN SIGNAL ADHESIVE ELECTRODES, XLTEK EMU40 EEG HEADBOX, MODEL PK1072
58
Total
53
Cleared
0
Denied
Excel Tech. , Ltd. has 53 FDA 510(k) cleared medical devices. Based in Oakville,Ontario, CA.
Historical record: 53 cleared submissions from 1985 to 2006. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Excel Tech. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Excel Tech. , Ltd.
58 devices
Cleared
Oct 04, 2006
XLTEK STIMULATOR PROBES, MODELS 105233, 105234, 105235, 105236, 105237 AND...
Ear, Nose, Throat
35d
Cleared
Aug 14, 2006
XLTEK CLEAN SIGNAL ADHESIVE ELECTRODES
Neurology
101d
Cleared
Apr 21, 2006
XLTEK EMU40 EEG HEADBOX, MODEL PK1072
Neurology
137d
Cleared
Feb 07, 2006
XLTEK NEUROPATH, MODEL PK1070
Neurology
99d
Cleared
Oct 28, 2005
XLTEK XCALIBUR EMG / LT, MODEL PK1P33, PK1059
Neurology
85d
Cleared
Aug 17, 2005
XLTEK CLEAR SIGNAL SUB-DERMAL NEEDLE, MODELS 102889, 102798, 102799, 102382
Neurology
13d
Cleared
Sep 16, 2004
XLTEK CONNEX IP HEADBOX, MODEL 1054
Neurology
30d
Cleared
Aug 27, 2004
XLTEK TREX MODEL#10309
Neurology
18d
Cleared
Aug 06, 2004
XLTEK PROTEKTOR STIMULATOR, MODELS 10247 & 10248
Neurology
175d
Cleared
Mar 12, 2004
EMU128S, MODEL EX-NW-128S
Neurology
28d
Cleared
Sep 10, 2002
XLTEK SLEEP SYSTEM
Neurology
78d
Cleared
Aug 13, 2002
96 CHANNEL EEG HEADBOX MODEL EMU96
Neurology
90d
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