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Vail Products, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K982783
VAIL 1000 ENCLOSED BED
October 5, 1998
K963622
VAIL 2000 ENCLOSED BED
May 7, 1997
K963589
VAIL 3000 BED ENCLOSURE
April 21, 1997
K963210
VAIL 100 PEDIATRIC CRIB
November 13, 1996