Medical Device Manufacturer · US , Tucson , AZ

Van Dellen, Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1987

Total

Cleared

Denied

Van Dellen, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Tucson, US.

Historical record: 7 cleared submissions from 1987 to 1988. Primary specialty: General Hospital.

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

Van Dellen, Ltd. 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 - Van Dellen, Ltd.

7 devices

1-7 of 7