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510k Database
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US
Hei, Inc.
Medical Device Manufacturer
·
US , Boulder , CO
Hei, Inc. - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2012
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hei, Inc.
General Hospital
✕
1
devices
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Cleared
Mar 21, 2012
HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM
K102900
·
LGZ
General Hospital
·
538d
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General Hospital
1