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510k Database
Manufacturers
BR
Timpel, Inc.
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Medical Device Manufacturer
·
BR , Sao Paulo-Sp
Timpel, Inc. - FDA 510(k) Cleared Devices
1 submissions
·
0 cleared
·
Since 2018
1
Total
0
Cleared
1
Denied
FDA 510(k) Regulatory Record - Timpel, Inc.
Anesthesiology
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devices
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Dec 20, 2018
Enlight 1810
DEN170072
·
QEB
Anesthesiology
·
447d
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