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Staodynamics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K852298TENS-AID STERILE ELECTRODES FOR POST-OP TENSJune 24, 1985
K843964TENS-AID PREMIUM ELECTRODESFebruary 25, 1985
K832988STAODYN EMS/PLUSNovember 22, 1983
K81328310D (TENS DEVICE)February 10, 1982
K813098TENS DEVICENovember 20, 1981
K811345INSIGHTJuly 10, 1981
K792529POINT LOCATOR STIMULATORFebruary 26, 1980
K792501PLS MINIFebruary 26, 1980
K800068ELECTRICAL MUSCLE STIMULATOR (EMS)February 5, 1980
K792502TENS 4100December 18, 1979
K792474TENS 4500December 13, 1979
K791087PORTABLE PULSE GALVANIC STIMULATOROctober 12, 1979
K790542ELECTRODES, STAODERM STERILEMay 23, 1979
K790904STAO-HOTPACKMay 18, 1979