Congratulations Moog Medical Devices for this achievement!
We are excited to announce we have received US FDA 510(k) Clearance for our CURLIN 8000 Ambulatory Infusion System. “The CURLIN 8000 is different as it was designed with a clear focus on our home care customers. This innovative infusion platform was developed through a collaborative effort with home care professionals to ensure that both the CURLIN 8000 pump and CURLIN RxManager software seamlessly integrate with current home care protocols and workflows.” - Mike Henderson, Vice President and General Manager of Moog’s Medical Devices division. Read more: https://lnkd.in/dJ5cd_7V