Medical Device Manufacturer · US , Flagstaff , AZ

Dailycare Biomedical, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2005

Total

Cleared

Denied

Dailycare Biomedical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Flagstaff, US.

Historical record: 5 cleared submissions from 2005 to 2018. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Dailycare Biomedical, Inc.

5 devices

1-5 of 5