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510k Database
Manufacturers
US
Kimble-Terumo, Inc.
Medical Device Manufacturer
·
US , Walker , MI
Kimble-Terumo, Inc. - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 1980
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kimble-Terumo, Inc.
Chemistry
✕
2
devices
1-2 of 2
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Cleared
May 14, 1980
PREZAPAK L ARTERIAL BLOOD SAMPLING KIT
K801015
·
GIM
Chemistry
·
15d
Cleared
Jan 17, 1980
VENOJECT AUTOSEP
K792587
·
JKA
Chemistry
·
31d
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Chemistry
2