Medical Device Manufacturer · US , Santa Monica , CA

Q'Apel - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Q'Apel has 2 FDA 510(k) cleared medical devices. Based in Santa Monica, US.

Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Q'Apel Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Q'Apel

2 devices

1-2 of 2