Q'Apel Medical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Q'Apel Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Fremont, US.
Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Q'Apel Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lakeshore Medical Device Consulting and Insight Medical, LLC.
4 devices