Home / Companies / Dyna-Med

Dyna-Med

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K884578POLARIX 2 AND POLARIX 2EFebruary 9, 1989
K884340AMX-110, AMX-II AND AMX-IIIJanuary 24, 1989
K863504OBSTETRICAL KITOctober 22, 1986
K760258BITE STICK, DYNAJuly 26, 1976