Rabar, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K844017MICROTENS 7757 T.E.N.S. STIMULATORNovember 30, 1984
K842414ECHO PULSE BURSTJuly 27, 1984
K821736ECHO-PULSE KM555December 9, 1982