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510k Database
Manufacturers
US
Cumes-Honikman Partnership
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Medical Device Manufacturer
·
US , Santa Barbara , CA
Cumes-Honikman Partnership - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1987
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cumes-Honikman Partnership
Gastroenterology & Urology
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1
devices
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Cleared
Dec 03, 1987
CUMEVAC
K874410
·
FFD
Gastroenterology & Urology
·
36d
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Gastroenterology & Urology
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