Medical Device Manufacturer · US , Carson City , NV

Dynatech/Nevada, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1990

Total

Cleared

Denied

Dynatech/Nevada, Inc. has 6 FDA 510(k) cleared medical devices. Based in Carson City, US.

Historical record: 6 cleared submissions from 1990 to 1995. Primary specialty: Cardiovascular.

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

Dynatech/Nevada, 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 - Dynatech/Nevada, Inc.

6 devices

1-6 of 6