QiG Group LLC

FDA Regulatory Profile

Summary

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

Recent Recalls

NumberClassProductDate
Z-1192-2016Class IIAlgostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)January 26, 2016
Z-1194-2016Class IIAlgostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400January 26, 2016
Z-1193-2016Class IIAlgostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)January 26, 2016