Medical Device Manufacturer · US , Boulder , CO

Dayspring Medical, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1996

Total

Cleared

Denied

Dayspring Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Boulder, US.

Historical record: 5 cleared submissions from 1996 to 1999. Primary specialty: Gastroenterology & Urology.

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

Dayspring Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dayspring Medical, Inc.

5 devices

1-5 of 5