Medical Device Manufacturer · US , Minneapolis , MN

Demstar Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987
1
Total
1
Cleared
0
Denied

Demstar Corp. has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Demstar Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Demstar Corp.

1 devices
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