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Qardio, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220106QardioArm 2June 15, 2022
K201644QardioCoreFebruary 28, 2021
K140067QARDIOARMJune 18, 2014