Medical Device Manufacturer · US , Mchenry , IL

Dupaco, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1977

Total

Cleared

Denied

Dupaco, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1977 to 2015.

Browse the FDA 510(k) cleared devices submitted by Dupaco, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Specialist, Inc. as regulatory consultant.

Dupaco, Inc. is one of 14224 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dupaco, Inc.

5 devices

1-5 of 5