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510k Database
Manufacturers
US
K & S Medicorp
Medical Device Manufacturer
·
US , Miami , FL
K & S Medicorp - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1986
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - K & S Medicorp
Cardiovascular
✕
2
devices
1-2 of 2
Filters
Cleared
May 13, 1986
TRANSCOR (TM) RADIO-STETHOSCOPE
K854772
·
DQD
Cardiovascular
·
165d
Cleared
May 09, 1986
SALTZMAN STETHOSCOPE HEAD
K854771
·
LDE
Cardiovascular
·
161d
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Cardiovascular
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Anesthesiology
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