Analog Devices, Inc.

FDA Regulatory Profile

Analog Devices, 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 December 10, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K243216Sensinel Cardiopulmonary Management (CPM) System (ADCP1100)December 10, 2024
K231086CPM SystemDecember 22, 2023