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Kamber Corporation
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Medical Device Manufacturer
·
US , Washington , DC
Kamber Corporation - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2005
Recent clearances:
ROBIN HOOD VEST
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kamber Corporation
General Hospital
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1
devices
1-1 of 1
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Cleared
Dec 08, 2005
ROBIN HOOD VEST
K051300
·
FRP
General Hospital
·
204d
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