# Analog Devices

- Location (FDA's records): Wilmington, MA
- FDA decisions: 3 (2023–2026): 3 510(k) clearances
- Names in FDA's records: Analog Devices (2); Analog Devices, Inc. (1)
- Product codes: MWI (3)
- 510(k) review time since 2016: median 219 days, against 239 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K260801: Sensinel Cardiopulmonary Management (CPM) System (Oct 16, 2026)
- K243216: Sensinel Cardiopulmonary Management (CPM) System (ADCP1100) (Dec 10, 2024)
- K231086: CPM System (Dec 22, 2023)

Source page: https://510kreport.com/company/analog-devices