Medical Device Manufacturer · US , Hopkins , MN

Nightware, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2020

Total

Cleared

Denied

Nightware, Inc. has 0 FDA 510(k) cleared medical devices. Based in Hopkins, US.

Active since 2020. Primary specialty: Neurology.

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

FDA 510(k) Regulatory Record - Nightware, Inc.

1 devices

1-1 of 1