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Pegabus Egerton, Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K945042
ELITE 3 LOW AIR LOSS BED
March 16, 1995
K945041
PARAGON PORTABLE
March 16, 1995