Wr Medical Electronics Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092809HRV ACQUIREOctober 19, 2010
K063560HILGER DUAL-STIM NERVE STIMULATORJanuary 5, 2007
K000574IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE)August 9, 2000
K992874Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEMNovember 18, 1999
K910624CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4January 17, 1992
K895838BRACKMANN EMG MONITORING SYSTEMMarch 27, 1990