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Search FDA 510(k) devices
510k Database
Manufacturers
US
Ipco Corp.
Medical Device Manufacturer
·
US , Mchenry , IL
Ipco Corp. - FDA 510(k) Cleared Devices
23 submissions
·
23 cleared
·
Since 1976
Official Website
23
Total
23
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ipco Corp.
Neurology
✕
2
devices
1-2 of 2
Filters
Cleared
Feb 11, 1980
TRU-PULSE PADS
K800117
·
GXY
Neurology
·
24d
Cleared
Mar 08, 1979
STIMULATOR, MODEL 1-600 ELECTRIC NERVR
K782164
·
GZJ
Neurology
·
76d
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23
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6
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4
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4
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3
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3
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2
General Hospital
1