Mego Afek

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K254267NanoPress 760A-BT (760A-BT)February 24, 2026
K230385Ballancer Platinum (1222)April 4, 2023
K072372PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICENovember 21, 2007
K060220PBS MODEL 701A COMPRESSION THERAPY DEVICEFebruary 9, 2006
K013331LYMPHA PRESS PLUS DEVICENovember 30, 2001
K810338LYMPHA PRESSOctober 20, 1981