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Dyna Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)July 28, 1997
K962181HARE MODEL 2000 EZ LOADER MODEL 95555August 1, 1996
K902503HARE FOLDING BACK EMERGENCY STRETCHERJune 26, 1990
K900671HARE EMERGENCY STRETCHER WITH WHEELSApril 23, 1990
K900670HARE EMERGENCY STRETCHERApril 23, 1990