Alcyone Lifesciences, Inc. is one of 18478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alcyone Lifesciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Alivio Ventricular Catheter and Flusher System (Alivio System), Alcyone MEMS Cannula (AMC) System
2
Total
2
Cleared
0
Denied
Alcyone Lifesciences, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lowell, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Alcyone Lifesciences, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Cyngus Regulatory.
FDA 510(k) Regulatory Record - Alcyone Lifesciences, Inc.
2 devices