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Motion Control, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K872040PHORESOR II (TM), MODEL PM700August 4, 1987
K862236MYOLAB II, MODEL ML-200August 7, 1986
K802642UTAH ARTIFICAL ARMNovember 12, 1980
K780310DERMATRON IONTOPHORESIS DEVICEJuly 31, 1978