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Annalise-Ai

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K250831Annalise EnterpriseApril 23, 2025
K213941Annalise Enterprise CXR Triage PneumothoraxFebruary 24, 2022