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Hausted, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943969MODEL 578 MOBILE SURGICAL STRETCHERJanuary 25, 1995
K945431MODEL 792 CONVERGE, MODEL 793 VISION 2000January 25, 1995