# Q'Apel

- Location (FDA's records): Santa Monica, CA
- FDA decisions: 2 (2018–2019): 2 510(k) clearances
- Product codes: DQY (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Penumbra, Inc.: 1 (https://510kreport.com/company/penumbra)
- Concentric Medical, Inc.: 1 (https://510kreport.com/company/concentric-medical)

## Firms that cite its devices most
- Q'Apel Medical, Inc.: 1 (https://510kreport.com/company/q-apel-medical)

## Its most-cited devices
- K181000: SelectFlex 072 Neurovascular Access System (2018), cited by 1

## Recent decisions
- K190749: 087 Balloon Guide Catheter System (Jul 15, 2019)
- K181000: SelectFlex 072 Neurovascular Access System (Sep 13, 2018)

Source page: https://510kreport.com/company/q-apel