Dyna-Med

FDA Regulatory Profile

Dyna-Med appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 9, 1989.

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