Everlife Medical Equipment Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K071624EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATORNovember 27, 2007
K071320EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211August 17, 2007
K070890EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507June 29, 2007