Medical Device Manufacturer · US , Oakland , CA

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

1 submissions · 1 cleared · Since 2021

1

Total

1

Cleared

0

Denied

Ziip, Inc. has 1 FDA 510(k) cleared medical devices. Based in Oakland, US.

Last cleared in 2021. Active since 2021. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Ziip, Inc.

1 devices

1-1 of 1

Cleared Sep 23, 2021

Neurology · 57d