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510k Database
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US
Somnitec, Inc.
Medical Device Manufacturer
·
US , Van Nuys , CA
Somnitec, Inc. - FDA 510(k) Cleared Devices
4 submissions
·
4 cleared
·
Since 1991
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Somnitec, Inc.
Anesthesiology
✕
1
devices
1-1 of 1
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Cleared
Jul 22, 1991
SOMNIPROBE(R) MODEL NUMBER 10093, MODIFICATION
K912234
·
BZG
Anesthesiology
·
66d
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Neurology
2
Cardiovascular
1
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