Medical Device Manufacturer · US , Chicago , IL

Synectics-Dantec - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1985
19
Total
18
Cleared
0
Denied

Synectics-Dantec has 18 FDA 510(k) cleared gastroenterology & urology devices. Based in Chicago, US.

Historical record: 18 cleared submissions from 1985 to 1997.

Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Synectics-Dantec
19 devices
1-12 of 19
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