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Apriomed AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K193268APrioCore PlusFebruary 27, 2020
K181756Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial NeedleDecember 18, 2018
K150625Morrison Steerable NeedleJune 9, 2015