Apriomed AB

FDA Regulatory Profile

Apriomed AB appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 27, 2020.

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