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510k Database
Manufacturers
US
Covidien LP
Medical Device Manufacturer
·
US , Mansfield , MA
Covidien LP - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 2009
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Covidien LP
Neurology
✕
1
devices
1-1 of 1
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Cleared
Apr 21, 2009
TENS/NMES/FES STIMULATING ELECTRODE
K083350
·
GXY
Neurology
·
159d
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3
Neurology
1
General & Plastic Surgery
1
Anesthesiology
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