Ibramed Equipamentos Medicos

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K210572Neurodyn V2.0, Neurodyn Aussie V2.0May 11, 2021
K131926THERMOPULSEJuly 24, 2014
K131917NEURODYN COMPACT, NEURODYN IIApril 29, 2014
K131309SONOPULSE COMPACT 1MHZ, SONOPULSE COMPACT 3MHZJanuary 27, 2014
K131629NEURODYN MULTIWAVE, AUSSIE SPORTNovember 26, 2013
K121369NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATORDecember 19, 2012