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Alcyone Lifesciences, Inc.

FDA Regulatory Profile

Alcyone Lifesciences, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 9, 2017.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K172006Alivio Ventricular Catheter and Flusher System (Alivio System)November 9, 2017
K150660Alcyone MEMS Cannula (AMC) SystemApril 16, 2015

FDA data resources