Q'Apel is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Q'Apel - FDA 510(k) Cleared Devices
Recent clearances: 087 Balloon Guide Catheter System, SelectFlex 072 Neurovascular Access System
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Lakeshore Medical Device Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Q'Apel
2 devices