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510k Database
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US
Aemed, Inc.
Medical Device Manufacturer
·
US , South Miami , FL
Aemed, Inc. - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 2008
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aemed, Inc.
Neurology
✕
2
devices
1-2 of 2
Filters
Cleared
Dec 18, 2014
StimPad OTC
K142686
·
NUH
Neurology
·
87d
Cleared
Mar 13, 2008
AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999
K071120
·
GZJ
Neurology
·
328d
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Neurology
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