Medical Device Manufacturer · US , Walker , MI

Transamerica Delaval, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1984

Total

Cleared

Denied

Transamerica Delaval, Inc. has 7 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 7 cleared submissions from 1984 to 1986. Primary specialty: Cardiovascular.

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

Transamerica Delaval, 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 - Transamerica Delaval, Inc.

7 devices

1-7 of 7