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510k Database
Manufacturers
DE
Pierenkemper GmbH
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Medical Device Manufacturer
·
DE , Ehringshausen
Pierenkemper GmbH - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2020
Recent clearances:
StimaWELL 120MTRS
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pierenkemper GmbH
Neurology
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1
devices
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Cleared
Aug 13, 2020
StimaWELL 120MTRS
K181645
·
GZJ
Neurology
·
783d
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Neurology
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